Deflazacort inactive ingredients by manufacturer
Wondering whether your Deflazacort 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 Deflazacort 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 50 of the 54 current Deflazacort products on the market today, from 11 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 Deflazacort? 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 Deflazacort products list lactose, a gluten source, soy, dyes or gelatin?
-
LactoseDiffers by manufacturer
40 of 50 checked products list lactose; 10 do not. See the products
Does not list it Aucta Biocon Cranbury Doppel Farmaceutici S.r.l. PTC Therapeutics Sun Upsher-Smith Zydus -
Wheat or gluten sourceNo checked product
No checked Deflazacort product lists a wheat or gluten source.
-
SoyNo checked product
No checked Deflazacort product lists soy.
-
Synthetic dyesNo checked product
No checked Deflazacort product lists synthetic dyes.
-
GelatinNo checked product
No checked Deflazacort product lists gelatin.
Also listed by some products: Corn 40 of 50 Benzyl alcohol 10 of 50 PEG or polysorbate 14 of 50 Sorbitol or mannitol 10 of 50
Find a version without it
Every current Deflazacort product and what its label lists
| Product | Lists | Inactive ingredients on the label |
|---|---|---|
| Amneal Pharmaceuticals NY LLC 4 products | ||
| 6 mg tabletNDC 60219-2282-01 | Still being read | Not read yet |
| 18 mg tabletNDC 60219-2283-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 60219-2284-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 60219-2285-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| Aucta Pharmaceuticals, Inc. 1 product | ||
| 22.75 mg/mL oral suspensionNDC 73289-0089-01 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 8 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, MAGNESIUM ALUMINUM SILICATE TYPE IIA, NONCRYSTALLIZING SORBITOL SOLUTION, POLYSORBATE 80, SILICON DIOXIDE, WATER |
| Aurobindo Pharma Limited 4 products | ||
| 6 mg tabletNDC 59651-0599-01 | Lactose Corn-derived Polyethylene glycol or polysorbate |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYSORBATE 80, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 59651-0600-30 | Lactose Corn-derived Polyethylene glycol or polysorbate |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYSORBATE 80, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 59651-0601-30 | Lactose Corn-derived Polyethylene glycol or polysorbate |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYSORBATE 80, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 59651-0602-30 | Lactose Corn-derived Polyethylene glycol or polysorbate |
Show 5 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, POLYSORBATE 80, SILICON DIOXIDE, STARCH, CORN |
| AvKARE 4 products | ||
| 6 mg tabletNDC 73190-0068-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 73190-0069-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 73190-0070-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 73190-0071-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| Biocon Pharma Inc. 1 product | ||
| 22.75 mg/mL oral suspensionNDC 70377-0188-21 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 7 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, MAGNESIUM ALUMINUM SILICATE, POLYSORBATE 80, SORBITOL SOLUTION, WATER |
| Cranbury Pharmaceuticals, LLC 1 product | ||
| 22.75 mg/mL oral suspensionNDC 27808-0249-01 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 7 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, MAGNESIUM ALUMINUM SILICATE TYPE IIA, POLYSORBATE 80, SORBITOL SOLUTION, WATER |
| Doppel Farmaceutici S.r.l. 10 products | ||
| 22.75 mg/mL oral suspensionNDC 81806-0213-13 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 6 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, MAGNESIUM ALUMINUM SILICATE TYPE IC, POLYSORBATE 80, SORBITOL SOLUTION |
| 22.75 mg/mL oral suspensionNDC 81806-0200-73 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 6 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, MAGNESIUM ALUMINUM SILICATE TYPE IC, POLYSORBATE 80, SORBITOL SOLUTION |
| 6 mg tabletNDC 81806-0174-10 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 6 mg tabletNDC 81806-0204-10 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 81806-0175-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 81806-0206-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 81806-0176-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 81806-0207-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 81806-0177-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 81806-0208-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| PTC Therapeutics, Inc. 5 products | ||
| 22.75 mg/mL oral suspensionNDC 52856-0505-22 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 7 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, MAGNESIUM ALUMINUM SILICATE, POLYSORBATE 80, SORBITOL, WATER |
| 6 mg tabletNDC 52856-0501-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, PREGELATINIZED CORN |
| 18 mg tabletNDC 52856-0502-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, PREGELATINIZED CORN |
| 30 mg tabletNDC 52856-0503-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, PREGELATINIZED CORN |
| 36 mg tabletNDC 52856-0504-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, PREGELATINIZED CORN |
| Sun Pharmaceutical Industries, Inc. 5 products | ||
| 22.75 mg/mL oral suspensionNDC 57664-0993-01 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 8 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, MAGNESIUM ALUMINUM SILICATE, POLYSORBATE 80, SODIUM HYDROXIDE, SORBITOL SOLUTION, WATER |
| 6 mg tabletNDC 70095-0040-01 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 70095-0041-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 70095-0042-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 70095-0043-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| Upsher-Smith Laboratories, LLC 9 products | ||
| 22.75 mg/mL oral suspensionNDC 00245-0813-13 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 7 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED, MAGNESIUM ALUMINUM SILICATE, POLYSORBATE 80, SORBITOL, WATER |
| 6 mg tabletNDC 00245-0814-11 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 6 mg tabletNDC 00832-0814-11 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 00245-0815-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 00832-0815-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 00245-0816-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 00832-0816-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 00245-0817-30 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 00832-0817-30 | Still being read | Not read yet |
| Zydus Pharmaceuticals (USA) Inc. 10 products | ||
| 22.75 mg/mL oral suspensionNDC 70710-2131-03 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 6 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, MAGNESIUM ALUMINUM SILICATE TYPE IC, POLYSORBATE 80, SORBITOL SOLUTION |
| 22.75 mg/mL oral suspensionNDC 70710-2007-03 | Benzyl alcohol Polyethylene glycol or polysorbate Sorbitol or mannitol |
Show 6 ingredientsACETIC ACID, BENZYL ALCOHOL, CARBOXYMETHYLCELLULOSE SODIUM, MAGNESIUM ALUMINUM SILICATE TYPE IC, POLYSORBATE 80, SORBITOL SOLUTION |
| 6 mg tabletNDC 70710-1749-01 | Still being read | Not read yet |
| 6 mg tabletNDC 70710-2051-01 | Still being read | Not read yet |
| 18 mg tabletNDC 70710-1750-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 18 mg tabletNDC 70710-2052-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 70710-2053-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 30 mg tabletNDC 70710-1751-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 70710-1752-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
| 36 mg tabletNDC 70710-2054-03 | Lactose Corn-derived |
Show 4 ingredientsLACTOSE MONOHYDRATE, MAGNESIUM STEARATE, SILICON DIOXIDE, STARCH, CORN |
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.
Deflazacort without lactose
Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 40 of 50 checked products list lactose; 10 do not.
Does not list lactose
- Aucta: 22.75 mg/mL oral suspension
- Biocon: 22.75 mg/mL oral suspension
- Cranbury: 22.75 mg/mL oral suspension
- Doppel Farmaceutici S.r.l.: 22.75 mg/mL oral suspension (NDC 81806-0213-13), 22.75 mg/mL oral suspension (NDC 81806-0200-73)
- PTC Therapeutics: 22.75 mg/mL oral suspension
- Sun: 22.75 mg/mL oral suspension
- Upsher-Smith: 22.75 mg/mL oral suspension
- Zydus: 22.75 mg/mL oral suspension (NDC 70710-2131-03), 22.75 mg/mL oral suspension (NDC 70710-2007-03)
Lists lactose
- Amneal: 18 mg tablet, 30 mg tablet, 36 mg tablet
- Aurobindo: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- AvKARE: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Doppel Farmaceutici S.r.l.: 6 mg tablet (NDC 81806-0174-10), 6 mg tablet (NDC 81806-0204-10), 18 mg tablet (NDC 81806-0175-30), 18 mg tablet (NDC 81806-0206-30), 30 mg tablet (NDC 81806-0176-30), 30 mg tablet (NDC 81806-0207-30), 36 mg tablet (NDC 81806-0177-30), 36 mg tablet (NDC 81806-0208-30)
- PTC Therapeutics: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Sun: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Upsher-Smith: 6 mg tablet (NDC 00245-0814-11), 6 mg tablet (NDC 00832-0814-11), 18 mg tablet (NDC 00245-0815-30), 18 mg tablet (NDC 00832-0815-30), 30 mg tablet (NDC 00245-0816-30), 30 mg tablet (NDC 00832-0816-30), 36 mg tablet
- Zydus: 18 mg tablet (NDC 70710-1750-03), 18 mg tablet (NDC 70710-2052-03), 30 mg tablet (NDC 70710-2053-03), 30 mg tablet (NDC 70710-1751-03), 36 mg tablet (NDC 70710-1752-03), 36 mg tablet (NDC 70710-2054-03)
Deflazacort without corn-derived ingredients
Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 40 of 50 checked products list corn-derived ingredients; 10 do not.
Does not list corn-derived ingredients
- Aucta: 22.75 mg/mL oral suspension
- Biocon: 22.75 mg/mL oral suspension
- Cranbury: 22.75 mg/mL oral suspension
- Doppel Farmaceutici S.r.l.: 22.75 mg/mL oral suspension (NDC 81806-0213-13), 22.75 mg/mL oral suspension (NDC 81806-0200-73)
- PTC Therapeutics: 22.75 mg/mL oral suspension
- Sun: 22.75 mg/mL oral suspension
- Upsher-Smith: 22.75 mg/mL oral suspension
- Zydus: 22.75 mg/mL oral suspension (NDC 70710-2131-03), 22.75 mg/mL oral suspension (NDC 70710-2007-03)
Lists corn-derived ingredients
- Amneal: 18 mg tablet, 30 mg tablet, 36 mg tablet
- Aurobindo: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- AvKARE: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Doppel Farmaceutici S.r.l.: 6 mg tablet (NDC 81806-0174-10), 6 mg tablet (NDC 81806-0204-10), 18 mg tablet (NDC 81806-0175-30), 18 mg tablet (NDC 81806-0206-30), 30 mg tablet (NDC 81806-0176-30), 30 mg tablet (NDC 81806-0207-30), 36 mg tablet (NDC 81806-0177-30), 36 mg tablet (NDC 81806-0208-30)
- PTC Therapeutics: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Sun: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Upsher-Smith: 6 mg tablet (NDC 00245-0814-11), 6 mg tablet (NDC 00832-0814-11), 18 mg tablet (NDC 00245-0815-30), 18 mg tablet (NDC 00832-0815-30), 30 mg tablet (NDC 00245-0816-30), 30 mg tablet (NDC 00832-0816-30), 36 mg tablet
- Zydus: 18 mg tablet (NDC 70710-1750-03), 18 mg tablet (NDC 70710-2052-03), 30 mg tablet (NDC 70710-2053-03), 30 mg tablet (NDC 70710-1751-03), 36 mg tablet (NDC 70710-1752-03), 36 mg tablet (NDC 70710-2054-03)
Deflazacort without benzyl alcohol
Benzyl alcohol: A preservative, mostly in injections and liquids; not for newborns. 10 of 50 checked products list benzyl alcohol; 40 do not.
Does not list benzyl alcohol
- Amneal: 18 mg tablet, 30 mg tablet, 36 mg tablet
- Aurobindo: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- AvKARE: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Doppel Farmaceutici S.r.l.: 6 mg tablet (NDC 81806-0174-10), 6 mg tablet (NDC 81806-0204-10), 18 mg tablet (NDC 81806-0175-30), 18 mg tablet (NDC 81806-0206-30), 30 mg tablet (NDC 81806-0176-30), 30 mg tablet (NDC 81806-0207-30), 36 mg tablet (NDC 81806-0177-30), 36 mg tablet (NDC 81806-0208-30)
- PTC Therapeutics: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Sun: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Upsher-Smith: 6 mg tablet (NDC 00245-0814-11), 6 mg tablet (NDC 00832-0814-11), 18 mg tablet (NDC 00245-0815-30), 18 mg tablet (NDC 00832-0815-30), 30 mg tablet (NDC 00245-0816-30), 30 mg tablet (NDC 00832-0816-30), 36 mg tablet
- Zydus: 18 mg tablet (NDC 70710-1750-03), 18 mg tablet (NDC 70710-2052-03), 30 mg tablet (NDC 70710-2053-03), 30 mg tablet (NDC 70710-1751-03), 36 mg tablet (NDC 70710-1752-03), 36 mg tablet (NDC 70710-2054-03)
Lists benzyl alcohol
- Aucta: 22.75 mg/mL oral suspension
- Biocon: 22.75 mg/mL oral suspension
- Cranbury: 22.75 mg/mL oral suspension
- Doppel Farmaceutici S.r.l.: 22.75 mg/mL oral suspension (NDC 81806-0213-13), 22.75 mg/mL oral suspension (NDC 81806-0200-73)
- PTC Therapeutics: 22.75 mg/mL oral suspension
- Sun: 22.75 mg/mL oral suspension
- Upsher-Smith: 22.75 mg/mL oral suspension
- Zydus: 22.75 mg/mL oral suspension (NDC 70710-2131-03), 22.75 mg/mL oral suspension (NDC 70710-2007-03)
Deflazacort without polyethylene glycol or polysorbate
Polyethylene glycol or polysorbate: PEG, macrogol or polysorbate; a rare cause of allergic reactions. 14 of 50 checked products list polyethylene glycol or polysorbate; 36 do not.
Does not list polyethylene glycol or polysorbate
- Amneal: 18 mg tablet, 30 mg tablet, 36 mg tablet
- AvKARE: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Doppel Farmaceutici S.r.l.: 6 mg tablet (NDC 81806-0174-10), 6 mg tablet (NDC 81806-0204-10), 18 mg tablet (NDC 81806-0175-30), 18 mg tablet (NDC 81806-0206-30), 30 mg tablet (NDC 81806-0176-30), 30 mg tablet (NDC 81806-0207-30), 36 mg tablet (NDC 81806-0177-30), 36 mg tablet (NDC 81806-0208-30)
- PTC Therapeutics: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Sun: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Upsher-Smith: 6 mg tablet (NDC 00245-0814-11), 6 mg tablet (NDC 00832-0814-11), 18 mg tablet (NDC 00245-0815-30), 18 mg tablet (NDC 00832-0815-30), 30 mg tablet (NDC 00245-0816-30), 30 mg tablet (NDC 00832-0816-30), 36 mg tablet
- Zydus: 18 mg tablet (NDC 70710-1750-03), 18 mg tablet (NDC 70710-2052-03), 30 mg tablet (NDC 70710-2053-03), 30 mg tablet (NDC 70710-1751-03), 36 mg tablet (NDC 70710-1752-03), 36 mg tablet (NDC 70710-2054-03)
Lists polyethylene glycol or polysorbate
- Aucta: 22.75 mg/mL oral suspension
- Aurobindo: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Biocon: 22.75 mg/mL oral suspension
- Cranbury: 22.75 mg/mL oral suspension
- Doppel Farmaceutici S.r.l.: 22.75 mg/mL oral suspension (NDC 81806-0213-13), 22.75 mg/mL oral suspension (NDC 81806-0200-73)
- PTC Therapeutics: 22.75 mg/mL oral suspension
- Sun: 22.75 mg/mL oral suspension
- Upsher-Smith: 22.75 mg/mL oral suspension
- Zydus: 22.75 mg/mL oral suspension (NDC 70710-2131-03), 22.75 mg/mL oral suspension (NDC 70710-2007-03)
Deflazacort without sorbitol or mannitol
Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 10 of 50 checked products list sorbitol or mannitol; 40 do not.
Does not list sorbitol or mannitol
- Amneal: 18 mg tablet, 30 mg tablet, 36 mg tablet
- Aurobindo: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- AvKARE: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Doppel Farmaceutici S.r.l.: 6 mg tablet (NDC 81806-0174-10), 6 mg tablet (NDC 81806-0204-10), 18 mg tablet (NDC 81806-0175-30), 18 mg tablet (NDC 81806-0206-30), 30 mg tablet (NDC 81806-0176-30), 30 mg tablet (NDC 81806-0207-30), 36 mg tablet (NDC 81806-0177-30), 36 mg tablet (NDC 81806-0208-30)
- PTC Therapeutics: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Sun: 6 mg tablet, 18 mg tablet, 30 mg tablet, 36 mg tablet
- Upsher-Smith: 6 mg tablet (NDC 00245-0814-11), 6 mg tablet (NDC 00832-0814-11), 18 mg tablet (NDC 00245-0815-30), 18 mg tablet (NDC 00832-0815-30), 30 mg tablet (NDC 00245-0816-30), 30 mg tablet (NDC 00832-0816-30), 36 mg tablet
- Zydus: 18 mg tablet (NDC 70710-1750-03), 18 mg tablet (NDC 70710-2052-03), 30 mg tablet (NDC 70710-2053-03), 30 mg tablet (NDC 70710-1751-03), 36 mg tablet (NDC 70710-1752-03), 36 mg tablet (NDC 70710-2054-03)
Lists sorbitol or mannitol
- Aucta: 22.75 mg/mL oral suspension
- Biocon: 22.75 mg/mL oral suspension
- Cranbury: 22.75 mg/mL oral suspension
- Doppel Farmaceutici S.r.l.: 22.75 mg/mL oral suspension (NDC 81806-0213-13), 22.75 mg/mL oral suspension (NDC 81806-0200-73)
- PTC Therapeutics: 22.75 mg/mL oral suspension
- Sun: 22.75 mg/mL oral suspension
- Upsher-Smith: 22.75 mg/mL oral suspension
- Zydus: 22.75 mg/mL oral suspension (NDC 70710-2131-03), 22.75 mg/mL oral suspension (NDC 70710-2007-03)
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 Deflazacort inactive ingredients
Is Deflazacort gluten-free?
Does Deflazacort contain lactose?
Does Deflazacort contain soy?
Is there a dye-free Deflazacort?
Does Deflazacort 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 Deflazacort products in the FDA's current NDC directory (openFDA), as of October 5, 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 Deflazacort guide