Desvenlafaxine inactive ingredients by manufacturer
Wondering whether your Desvenlafaxine has lactose, gluten, soy, a dye or gelatin in it? The medicine is the same, but the fillers, coatings and colors differ from one company to the next. This page shows what each Desvenlafaxine product's FDA label lists, so you can find a version that leaves out what you avoid and ask your pharmacist for it by its NDC.
We have read the FDA labels of 64 of the 68 current Desvenlafaxine products on the market today, from 23 companies listing it with the FDA, and lined them up side by side. 4 are still being read and will appear on a later visit.
Ask about your bottle
Is there something in your Desvenlafaxine? Ask in plain words.
Name the company, strength or the NDC on your bottle and the ingredient you avoid. The answer comes only from the FDA labels on this page.
Answers are drawn from the FDA label data on this page and checked against it. They are not medical advice: confirm with your pharmacist before relying on them.
The short answer
Which Desvenlafaxine products list lactose, a gluten source, soy, dyes or gelatin?
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LactoseNo checked product
No checked Desvenlafaxine product lists lactose.
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Wheat or gluten sourceNo checked product
No checked Desvenlafaxine product lists a wheat or gluten source.
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SoyNo checked product
No checked Desvenlafaxine product lists soy.
-
Synthetic dyesDiffers by manufacturer
20 of 64 checked products list synthetic dyes; 44 do not. See the products
Does not list it A-S Medication Solutions Actavis Advagen Alembic Breckenridge Bryant Ranch Prepack Coupler Direct Rx Direct_Rx Lupin Macleods Marlex NorthStar Rx Preferred Pharmaceutical, Inc. Preferred Pharmaceuticals Inc. Proficient Rx Slate Run Sun Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer -
GelatinNo checked product
No checked Desvenlafaxine product lists gelatin.
Also listed by some products: Titanium dioxide 61 of 64 Carmine or shellac 2 of 64 Propylene glycol 2 of 64 PEG or polysorbate 64 of 64
Find a version without it
Every current Desvenlafaxine product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| A-S Medication Solutions 8 products | ||
| 25 mg extended-release tabletNDC 50090-5274-00 | Still being read | Not read yet |
| 25 mg extended-release tabletNDC 50090-6738-00 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsCELLULOSE, MICROCRYSTALLINE, CI 77491, CI 77492, CI 77499, HYDROXYPROPYL METHYLCELLULOSE, MAGNESIUM STEARATE, PEG-20M, POLYVINYL ALCOHOL GRAFT POLYETHYLENE GLYCOL COPOLYMER (3:1; 45000 MW), SILICA, TALC, TITANIUM DIOXIDE |
| 25 mg extended-release tabletNDC 50090-7190-00 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsCELLULOSE, MICROCRYSTALLINE, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYDROXYPROPYL METHYLCELLULOSE, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, TALC, TITANIUM DIOXIDE |
| 25 mg extended-release tabletNDC 50090-7468-00 | Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, CI 77499, CI 77891, FERRIC OXIDE RED, HYDROXYPROPYL METHYLCELLULOSE, MAGNESIUM STEARATE, PEG-75, POLYVINYL ALCOHOL, SILICA, TALC |
| 50 mg extended-release tabletNDC 50090-5293-00 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsFERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 50090-7737-00 | Synthetic dyes Polyethylene glycol or polysorbate |
Show 9 ingredientsCELLULOSE, MICROCRYSTALLINE, CI 77891, HYPROMELLOSES, KI5, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, RED 40, TALC |
| 50 mg extended-release tabletNDC 50090-4806-00 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsCELLULOSE, MICROCRYSTALLINE, FD&C YELLOW NO. 6, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 1000, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K30, RED 40, SILICA, SODIUM STEARYL FUMARATE, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 50090-6894-00 | Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, CI 77491, CI 77492, CI 77891, HYDROXYPROPYL METHYLCELLULOSE, MAGNESIUM STEARATE, PEG-75, POLYVINYL ALCOHOL, SILICA, TALC |
| Actavis Pharma, Inc. 3 products | ||
| 25 mg extended-release tabletNDC 00591-4060-30 | Still being read | Not read yet |
| 50 mg extended-release tabletNDC 00591-3659-30 | Titanium dioxide Carmine or shellac Propylene glycol Polyethylene glycol or polysorbate |
Show 15 ingredientsAMMONIA, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE OXIDE 100000, POLYVINYL ALCOHOL, UNSPECIFIED, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 00591-3660-30 | Titanium dioxide Carmine or shellac Propylene glycol Polyethylene glycol or polysorbate |
Show 15 ingredientsAMMONIA, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE OXIDE 100000, POLYVINYL ALCOHOL, UNSPECIFIED, PROPYLENE GLYCOL, SHELLAC, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Advagen Pharma Ltd 3 products | ||
| 25 mg extended-release tabletNDC 72888-0175-00 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 72888-0143-00 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 72888-0144-00 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| Alembic Pharmaceuticals Limited 5 products | ||
| 25 mg extended-release tabletNDC 46708-0542-10 | Still being read | Not read yet |
| 50 mg extended-release tabletNDC 46708-0152-30 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsALGINIC ACID, CITRIC ACID MONOHYDRATE, FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K30, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 46708-0540-10 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsFERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 46708-0153-30 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsALGINIC ACID, CITRIC ACID MONOHYDRATE, FERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K30, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 46708-0541-10 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| American Health Packaging 1 product | ||
| 50 mg extended-release tabletNDC 60687-0607-21 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K30, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC, TITANIUM DIOXIDE |
| Breckenridge Pharmaceutical, Inc 3 products | ||
| 25 mg extended-release tabletNDC 51991-0006-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 51991-0311-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsFERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 51991-0312-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| Bryant Ranch Prepack 14 products | ||
| 25 mg extended-release tabletNDC 71335-2490-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 25 mg extended-release tabletNDC 71335-2130-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 25 mg extended-release tabletNDC 71335-1975-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE OXIDE 900000, POLYVINYL ALCOHOL GRAFT POLYETHYLENE GLYCOL COPOLYMER (3:1; 45000 MW), SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 25 mg extended-release tabletNDC 63629-7524-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 13 ingredientsFD&C BLUE NO. 1, FD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K30, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC, TITANIUM DIOXIDE |
| 25 mg extended-release tabletNDC 71335-2494-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 63629-7525-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsFERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 71335-2575-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 71335-1753-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE OXIDE 900000, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 71335-1150-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 71335-1700-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K30, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 63629-7559-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 71335-2512-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 71335-1815-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsD&C RED NO. 27 ALUMINUM LAKE, FD&C BLUE NO. 2, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE OXIDE 900000, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 71335-1331-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFD&C YELLOW NO. 6, FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Coupler LLC 1 product | ||
| 100 mg extended-release tabletNDC 67046-1545-03 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| Direct Rx 1 product | ||
| 50 mg extended-release tabletNDC 72189-0147-28 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsCELLULOSE, MICROCRYSTALLINE, FERRIC OXIDE RED, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| Direct_rx 1 product | ||
| 50 mg extended-release tabletNDC 72189-0567-28 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| Direct_Rx 1 product | ||
| 50 mg extended-release tabletNDC 61919-0882-28 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Hikma Pharmaceuticals USA Inc. 3 products | ||
| 25 mg extended-release tabletNDC 00054-0603-13 | Still being read | Not read yet |
| 50 mg extended-release tabletNDC 00054-0400-13 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K30, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 00054-0401-13 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE 2208 (100 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 1000, POLYVINYL ALCOHOL, UNSPECIFIED, POVIDONE K30, SILICON DIOXIDE, SODIUM STEARYL FUMARATE, TALC, TITANIUM DIOXIDE |
| Lupin Pharmaceuticals, Inc. 3 products | ||
| 25 mg extended-release tabletNDC 68180-0604-02 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, FERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 68180-0592-02 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 68180-0593-02 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, FD&C YELLOW NO. 6, FERRIC OXIDE RED, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Macleods Pharmaceuticals Limited 2 products | ||
| 50 mg extended-release tabletNDC 33342-0388-07 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsCELLULOSE, MICROCRYSTALLINE, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 400, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 33342-0389-07 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsCELLULOSE, MICROCRYSTALLINE, FD&C YELLOW NO. 6, FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 400, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Marlex Pharmaceuticals, Inc. 2 products | ||
| 50 mg extended-release tabletNDC 10135-0821-10 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsETHYLCELLULOSE (100 MPA.S), FERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%), HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 10135-0822-10 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsETHYLCELLULOSE (100 MPA.S), FERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%), HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| NorthStar Rx LLC 3 products | ||
| 25 mg extended-release tabletNDC 72603-0555-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 72603-0556-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 72603-0557-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| NuCare Pharmaceuticals,Inc. 1 product | ||
| 50 mg extended-release tabletNDC 68071-3790-03 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| Preferred Pharmaceutical, Inc. 1 product | ||
| 50 mg extended-release tabletNDC 68788-7194-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 8 ingredientsFERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 6000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| Preferred Pharmaceuticals Inc. 3 products | ||
| 50 mg extended-release tabletNDC 68788-8760-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C RED NO. 40, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 68788-7175-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 68788-8556-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsFD&C YELLOW NO. 6, FERRIC OXIDE RED, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYVINYL ALCOHOL, UNSPECIFIED, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Proficient Rx LP 1 product | ||
| 100 mg extended-release tabletNDC 71205-0586-30 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 8000, POVIDONE K90, TALC, TITANIUM DIOXIDE |
| Slate Run Pharmaceuticals, LLC 3 products | ||
| 25 mg extended-release tabletNDC 70436-0036-04 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, FERROSOFERRIC OXIDE, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE OXIDE 900000, POLYVINYL ALCOHOL GRAFT POLYETHYLENE GLYCOL COPOLYMER (3:1; 45000 MW), SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 70436-0012-04 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE OXIDE 900000, POLYVINYL ALCOHOL, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 70436-0013-03 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 12 ingredientsD&C RED NO. 27 ALUMINUM LAKE, FD&C BLUE NO. 2, FD&C YELLOW NO. 6, HYPROMELLOSE, UNSPECIFIED, MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL 3350, POLYETHYLENE OXIDE 900000, POLYVINYL ALCOHOL, SILICON DIOXIDE, TALC, TITANIUM DIOXIDE |
| Sun Pharmaceutical Industries, Inc. 2 products | ||
| 50 mg extended-release tabletNDC 63304-0191-30 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 10 ingredientsALGINIC ACID, CELLULOSE, MICROCRYSTALLINE, CITRIC ACID MONOHYDRATE, FERRIC OXIDE RED, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 6000, POVIDONE K30, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 63304-0192-30 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 11 ingredientsALGINIC ACID, CELLULOSE, MICROCRYSTALLINE, CITRIC ACID MONOHYDRATE, FERRIC OXIDE RED, FERROSOFERRIC OXIDE, HYPROMELLOSES, MAGNESIUM STEARATE, POLYETHYLENE GLYCOL 8000, POVIDONE K30, TALC, TITANIUM DIOXIDE |
| Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. 3 products | ||
| 25 mg extended-release tabletNDC 00008-1210-30 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE 2208 (15000 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 50 mg extended-release tabletNDC 00008-1211-01 | Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFERRIC OXIDE RED, FERRIC OXIDE YELLOW, HYPROMELLOSE 2208 (15000 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
| 100 mg extended-release tabletNDC 00008-1222-01 | Synthetic dyes Titanium dioxide Polyethylene glycol or polysorbate |
Show 9 ingredientsFD&C YELLOW NO. 6, FERRIC OXIDE YELLOW, HYPROMELLOSE 2208 (15000 MPA.S), MAGNESIUM STEARATE, MICROCRYSTALLINE CELLULOSE, POLYETHYLENE GLYCOL, UNSPECIFIED, POLYVINYL ALCOHOL, UNSPECIFIED, TALC, TITANIUM DIOXIDE |
A product with none of these listed is not certified to be without them: the label says what the manufacturer declared, and the source of a starch or a flavor is often not stated. The companies are the FDA's labelers, which include repackagers and distributors selling another company's product under their own label. The NDC opens the product's own page, with the full label and its inactive-ingredient notes.
Desvenlafaxine without synthetic dyes
Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 20 of 64 checked products list synthetic dyes; 44 do not.
Does not list synthetic dyes
- A-S Medication Solutions: 25 mg extended-release tablet (NDC 50090-6738-00), 25 mg extended-release tablet (NDC 50090-7190-00), 25 mg extended-release tablet (NDC 50090-7468-00), 50 mg extended-release tablet (NDC 50090-5293-00), 50 mg extended-release tablet (NDC 50090-6894-00)
- Actavis: 50 mg extended-release tablet, 100 mg extended-release tablet
- Advagen: 25 mg extended-release tablet, 100 mg extended-release tablet
- Alembic: 50 mg extended-release tablet (NDC 46708-0152-30), 50 mg extended-release tablet (NDC 46708-0540-10), 100 mg extended-release tablet (NDC 46708-0153-30), 100 mg extended-release tablet (NDC 46708-0541-10)
- Breckenridge: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Bryant Ranch Prepack: 25 mg extended-release tablet (NDC 71335-2490-01), 25 mg extended-release tablet (NDC 71335-2130-01), 25 mg extended-release tablet (NDC 71335-1975-01), 25 mg extended-release tablet (NDC 71335-2494-01), 50 mg extended-release tablet (NDC 63629-7525-01), 50 mg extended-release tablet (NDC 71335-1753-01), 50 mg extended-release tablet (NDC 71335-1150-01), 100 mg extended-release tablet (NDC 63629-7559-01), 100 mg extended-release tablet (NDC 71335-2512-01)
- Coupler: 100 mg extended-release tablet
- Direct Rx: 50 mg extended-release tablet
- Direct_Rx: 50 mg extended-release tablet
- Lupin: 25 mg extended-release tablet, 50 mg extended-release tablet
- Macleods: 50 mg extended-release tablet
- Marlex: 50 mg extended-release tablet, 100 mg extended-release tablet
- NorthStar Rx: 25 mg extended-release tablet, 100 mg extended-release tablet
- Preferred Pharmaceutical, Inc.: 50 mg extended-release tablet
- Preferred Pharmaceuticals Inc.: 100 mg extended-release tablet
- Proficient Rx: 100 mg extended-release tablet
- Slate Run: 25 mg extended-release tablet, 50 mg extended-release tablet
- Sun: 50 mg extended-release tablet, 100 mg extended-release tablet
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer: 25 mg extended-release tablet, 50 mg extended-release tablet
Lists synthetic dyes
- A-S Medication Solutions: 50 mg extended-release tablet (NDC 50090-7737-00), 50 mg extended-release tablet (NDC 50090-4806-00)
- Advagen: 50 mg extended-release tablet
- American Health Packaging: 50 mg extended-release tablet
- Bryant Ranch Prepack: 25 mg extended-release tablet, 50 mg extended-release tablet (NDC 71335-2575-01), 50 mg extended-release tablet (NDC 71335-1700-01), 100 mg extended-release tablet (NDC 71335-1815-01), 100 mg extended-release tablet (NDC 71335-1331-01)
- Direct_rx: 50 mg extended-release tablet
- Hikma: 50 mg extended-release tablet, 100 mg extended-release tablet
- Lupin: 100 mg extended-release tablet
- Macleods: 100 mg extended-release tablet
- NorthStar Rx: 50 mg extended-release tablet
- NuCare: 50 mg extended-release tablet
- Preferred Pharmaceuticals Inc.: 50 mg extended-release tablet, 100 mg extended-release tablet
- Slate Run: 100 mg extended-release tablet
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer: 100 mg extended-release tablet
Desvenlafaxine without titanium dioxide
Titanium dioxide: A white colorant some people choose to avoid. 61 of 64 checked products list titanium dioxide; 3 do not.
Does not list titanium dioxide
Lists titanium dioxide
- A-S Medication Solutions: 25 mg extended-release tablet (NDC 50090-6738-00), 25 mg extended-release tablet (NDC 50090-7190-00), 50 mg extended-release tablet (NDC 50090-5293-00), 50 mg extended-release tablet (NDC 50090-4806-00)
- Actavis: 50 mg extended-release tablet, 100 mg extended-release tablet
- Advagen: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Alembic: 50 mg extended-release tablet (NDC 46708-0152-30), 50 mg extended-release tablet (NDC 46708-0540-10), 100 mg extended-release tablet (NDC 46708-0153-30), 100 mg extended-release tablet (NDC 46708-0541-10)
- American Health Packaging: 50 mg extended-release tablet
- Breckenridge: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Bryant Ranch Prepack: 25 mg extended-release tablet (NDC 71335-2490-01), 25 mg extended-release tablet (NDC 71335-2130-01), 25 mg extended-release tablet (NDC 71335-1975-01), 25 mg extended-release tablet (NDC 63629-7524-01), 25 mg extended-release tablet (NDC 71335-2494-01), 50 mg extended-release tablet (NDC 63629-7525-01), 50 mg extended-release tablet (NDC 71335-2575-01), 50 mg extended-release tablet (NDC 71335-1753-01), 50 mg extended-release tablet (NDC 71335-1150-01), 50 mg extended-release tablet (NDC 71335-1700-01), 100 mg extended-release tablet (NDC 63629-7559-01), 100 mg extended-release tablet (NDC 71335-2512-01), 100 mg extended-release tablet (NDC 71335-1815-01), 100 mg extended-release tablet (NDC 71335-1331-01)
- Coupler: 100 mg extended-release tablet
- Direct Rx: 50 mg extended-release tablet
- Direct_rx: 50 mg extended-release tablet
- Direct_Rx: 50 mg extended-release tablet
- Hikma: 50 mg extended-release tablet, 100 mg extended-release tablet
- Lupin: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Macleods: 50 mg extended-release tablet, 100 mg extended-release tablet
- Marlex: 50 mg extended-release tablet, 100 mg extended-release tablet
- NorthStar Rx: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- NuCare: 50 mg extended-release tablet
- Preferred Pharmaceutical, Inc.: 50 mg extended-release tablet
- Preferred Pharmaceuticals Inc.: 50 mg extended-release tablet, 100 mg extended-release tablet (NDC 68788-7175-01), 100 mg extended-release tablet (NDC 68788-8556-01)
- Proficient Rx: 100 mg extended-release tablet
- Slate Run: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Sun: 50 mg extended-release tablet, 100 mg extended-release tablet
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
Desvenlafaxine without carmine or shellac
Carmine or shellac: insect-derived red colorant or coating glaze. 2 of 64 checked products list carmine or shellac; 62 do not.
Does not list carmine or shellac
- A-S Medication Solutions: 25 mg extended-release tablet (NDC 50090-6738-00), 25 mg extended-release tablet (NDC 50090-7190-00), 25 mg extended-release tablet (NDC 50090-7468-00), 50 mg extended-release tablet (NDC 50090-5293-00), 50 mg extended-release tablet (NDC 50090-7737-00), 50 mg extended-release tablet (NDC 50090-4806-00), 50 mg extended-release tablet (NDC 50090-6894-00)
- Advagen: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Alembic: 50 mg extended-release tablet (NDC 46708-0152-30), 50 mg extended-release tablet (NDC 46708-0540-10), 100 mg extended-release tablet (NDC 46708-0153-30), 100 mg extended-release tablet (NDC 46708-0541-10)
- American Health Packaging: 50 mg extended-release tablet
- Breckenridge: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Bryant Ranch Prepack: 25 mg extended-release tablet (NDC 71335-2490-01), 25 mg extended-release tablet (NDC 71335-2130-01), 25 mg extended-release tablet (NDC 71335-1975-01), 25 mg extended-release tablet (NDC 63629-7524-01), 25 mg extended-release tablet (NDC 71335-2494-01), 50 mg extended-release tablet (NDC 63629-7525-01), 50 mg extended-release tablet (NDC 71335-2575-01), 50 mg extended-release tablet (NDC 71335-1753-01), 50 mg extended-release tablet (NDC 71335-1150-01), 50 mg extended-release tablet (NDC 71335-1700-01), 100 mg extended-release tablet (NDC 63629-7559-01), 100 mg extended-release tablet (NDC 71335-2512-01), 100 mg extended-release tablet (NDC 71335-1815-01), 100 mg extended-release tablet (NDC 71335-1331-01)
- Coupler: 100 mg extended-release tablet
- Direct Rx: 50 mg extended-release tablet
- Direct_rx: 50 mg extended-release tablet
- Direct_Rx: 50 mg extended-release tablet
- Hikma: 50 mg extended-release tablet, 100 mg extended-release tablet
- Lupin: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Macleods: 50 mg extended-release tablet, 100 mg extended-release tablet
- Marlex: 50 mg extended-release tablet, 100 mg extended-release tablet
- NorthStar Rx: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- NuCare: 50 mg extended-release tablet
- Preferred Pharmaceutical, Inc.: 50 mg extended-release tablet
- Preferred Pharmaceuticals Inc.: 50 mg extended-release tablet, 100 mg extended-release tablet (NDC 68788-7175-01), 100 mg extended-release tablet (NDC 68788-8556-01)
- Proficient Rx: 100 mg extended-release tablet
- Slate Run: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Sun: 50 mg extended-release tablet, 100 mg extended-release tablet
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
Lists carmine or shellac
Desvenlafaxine without propylene glycol
Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 2 of 64 checked products list propylene glycol; 62 do not.
Does not list propylene glycol
- A-S Medication Solutions: 25 mg extended-release tablet (NDC 50090-6738-00), 25 mg extended-release tablet (NDC 50090-7190-00), 25 mg extended-release tablet (NDC 50090-7468-00), 50 mg extended-release tablet (NDC 50090-5293-00), 50 mg extended-release tablet (NDC 50090-7737-00), 50 mg extended-release tablet (NDC 50090-4806-00), 50 mg extended-release tablet (NDC 50090-6894-00)
- Advagen: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Alembic: 50 mg extended-release tablet (NDC 46708-0152-30), 50 mg extended-release tablet (NDC 46708-0540-10), 100 mg extended-release tablet (NDC 46708-0153-30), 100 mg extended-release tablet (NDC 46708-0541-10)
- American Health Packaging: 50 mg extended-release tablet
- Breckenridge: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Bryant Ranch Prepack: 25 mg extended-release tablet (NDC 71335-2490-01), 25 mg extended-release tablet (NDC 71335-2130-01), 25 mg extended-release tablet (NDC 71335-1975-01), 25 mg extended-release tablet (NDC 63629-7524-01), 25 mg extended-release tablet (NDC 71335-2494-01), 50 mg extended-release tablet (NDC 63629-7525-01), 50 mg extended-release tablet (NDC 71335-2575-01), 50 mg extended-release tablet (NDC 71335-1753-01), 50 mg extended-release tablet (NDC 71335-1150-01), 50 mg extended-release tablet (NDC 71335-1700-01), 100 mg extended-release tablet (NDC 63629-7559-01), 100 mg extended-release tablet (NDC 71335-2512-01), 100 mg extended-release tablet (NDC 71335-1815-01), 100 mg extended-release tablet (NDC 71335-1331-01)
- Coupler: 100 mg extended-release tablet
- Direct Rx: 50 mg extended-release tablet
- Direct_rx: 50 mg extended-release tablet
- Direct_Rx: 50 mg extended-release tablet
- Hikma: 50 mg extended-release tablet, 100 mg extended-release tablet
- Lupin: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Macleods: 50 mg extended-release tablet, 100 mg extended-release tablet
- Marlex: 50 mg extended-release tablet, 100 mg extended-release tablet
- NorthStar Rx: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- NuCare: 50 mg extended-release tablet
- Preferred Pharmaceutical, Inc.: 50 mg extended-release tablet
- Preferred Pharmaceuticals Inc.: 50 mg extended-release tablet, 100 mg extended-release tablet (NDC 68788-7175-01), 100 mg extended-release tablet (NDC 68788-8556-01)
- Proficient Rx: 100 mg extended-release tablet
- Slate Run: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Sun: 50 mg extended-release tablet, 100 mg extended-release tablet
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
Lists propylene glycol
Desvenlafaxine and polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. Every checked Desvenlafaxine product (64) lists polyethylene glycol or polysorbate.
Lists polyethylene glycol or polysorbate
- A-S Medication Solutions: 25 mg extended-release tablet (NDC 50090-6738-00), 25 mg extended-release tablet (NDC 50090-7190-00), 25 mg extended-release tablet (NDC 50090-7468-00), 50 mg extended-release tablet (NDC 50090-5293-00), 50 mg extended-release tablet (NDC 50090-7737-00), 50 mg extended-release tablet (NDC 50090-4806-00), 50 mg extended-release tablet (NDC 50090-6894-00)
- Actavis: 50 mg extended-release tablet, 100 mg extended-release tablet
- Advagen: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Alembic: 50 mg extended-release tablet (NDC 46708-0152-30), 50 mg extended-release tablet (NDC 46708-0540-10), 100 mg extended-release tablet (NDC 46708-0153-30), 100 mg extended-release tablet (NDC 46708-0541-10)
- American Health Packaging: 50 mg extended-release tablet
- Breckenridge: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Bryant Ranch Prepack: 25 mg extended-release tablet (NDC 71335-2490-01), 25 mg extended-release tablet (NDC 71335-2130-01), 25 mg extended-release tablet (NDC 71335-1975-01), 25 mg extended-release tablet (NDC 63629-7524-01), 25 mg extended-release tablet (NDC 71335-2494-01), 50 mg extended-release tablet (NDC 63629-7525-01), 50 mg extended-release tablet (NDC 71335-2575-01), 50 mg extended-release tablet (NDC 71335-1753-01), 50 mg extended-release tablet (NDC 71335-1150-01), 50 mg extended-release tablet (NDC 71335-1700-01), 100 mg extended-release tablet (NDC 63629-7559-01), 100 mg extended-release tablet (NDC 71335-2512-01), 100 mg extended-release tablet (NDC 71335-1815-01), 100 mg extended-release tablet (NDC 71335-1331-01)
- Coupler: 100 mg extended-release tablet
- Direct Rx: 50 mg extended-release tablet
- Direct_rx: 50 mg extended-release tablet
- Direct_Rx: 50 mg extended-release tablet
- Hikma: 50 mg extended-release tablet, 100 mg extended-release tablet
- Lupin: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Macleods: 50 mg extended-release tablet, 100 mg extended-release tablet
- Marlex: 50 mg extended-release tablet, 100 mg extended-release tablet
- NorthStar Rx: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- NuCare: 50 mg extended-release tablet
- Preferred Pharmaceutical, Inc.: 50 mg extended-release tablet
- Preferred Pharmaceuticals Inc.: 50 mg extended-release tablet, 100 mg extended-release tablet (NDC 68788-7175-01), 100 mg extended-release tablet (NDC 68788-8556-01)
- Proficient Rx: 100 mg extended-release tablet
- Slate Run: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
- Sun: 50 mg extended-release tablet, 100 mg extended-release tablet
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer: 25 mg extended-release tablet, 50 mg extended-release tablet, 100 mg extended-release tablet
At the pharmacy counter
How to use this at the pharmacy counter
- Pick the company whose list suits you and copy the NDC from the table. Many pharmacies order from wholesalers that carry several companies' versions and can request a particular one if you ask before the prescription is filled; some buy from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check.
- Treat "does not list" as exactly that. The label is what the manufacturer declared; a flavor or a starch may have an unstated source, and lines change. For celiac disease or a serious allergy, ask the manufacturer's medical information line for a written statement about the lot you have.
- Check the bottle each refill. A different company usually means a different shape, color and inactive-ingredient list; the pharmacist can tell you who made it, and the two-NDC comparison shows the difference line by line.
- If you need one company's version kept constant, ask your prescriber to write that company or the NDC on the prescription and tell the pharmacy you need it held. Rules vary by state and plan, so confirm with the pharmacist.
Common questions about Desvenlafaxine inactive ingredients
Is Desvenlafaxine gluten-free?
Does Desvenlafaxine contain lactose?
Does Desvenlafaxine contain soy?
Is there a dye-free Desvenlafaxine?
Does Desvenlafaxine contain gelatin?
Why do the inactive ingredients differ between manufacturers?
Can my pharmacy give me a specific manufacturer's version?
How current is this list?
Sources: the products are the finished Desvenlafaxine products in the FDA's current NDC directory (openFDA), as of October 6, 2026; each inactive-ingredient list is the manufacturer's FDA Structured Product Label via DailyMed, as our label sync last read it. The concern groups are HelloPharmacist's classification of the names the label declares. Educational information only, not medical advice; confirm with your pharmacist before relying on a list. ← Back to the Desvenlafaxine guide