Inactive ingredients by manufacturer

Buprenorphine inactive ingredients by manufacturer

Wondering whether your Buprenorphine 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 Buprenorphine 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 83 of the 106 current Buprenorphine products on the market today, from 32 companies listing it with the FDA, and lined them up side by side. 22 are still being read and will appear on a later visit. 1 could not be linked to a current label.

Ask about your bottle

Is there something in your Buprenorphine? 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 Buprenorphine products list lactose, a gluten source, soy, dyes or gelatin?

  1. LactoseDiffers by manufacturer
  2. Wheat or gluten sourceNo checked product

    No checked Buprenorphine product lists a wheat or gluten source.

  3. SoyDiffers by manufacturer
  4. Synthetic dyesDiffers by manufacturer
  5. GelatinNo checked product

    No checked Buprenorphine product lists gelatin.

Also listed by some products: Corn 46 of 83 Titanium dioxide 4 of 83 Alcohol 2 of 83 Propylene glycol 4 of 83 Sorbitol or mannitol 46 of 83 Sugar 4 of 83

Find a version without it

Every current Buprenorphine product and what its label lists

Hide products that list:

ProductListsInactive ingredients on the label
A-S Medication Solutions 2 products
8 mg sublingual tabletNDC 50090-5805-00 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

Anhydrous Citric Acid, CROSPOVIDONE, Lactose monohydrate, Magnesium Stearate, Mannitol, Povidone K30, Starch, Corn, Trisodium Citrate Dihydrate

8 mg sublingual tabletNDC 50090-7559-00 Lactose Corn-derived Sorbitol or mannitol
Show 7 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MANNITOL, POVIDONE K30, SODIUM STEARYL FUMARATE, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Actavis Pharma, Inc. 2 products
2 mg sublingual tabletNDC 00228-3156-03 Lactose Corn-derived Synthetic dyes Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (15 MPA.S AT 5%), FD&C YELLOW NO. 6, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 00228-3153-03 Lactose Corn-derived Synthetic dyes Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (15 MPA.S AT 5%), FD&C YELLOW NO. 6, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Advagen Pharma Ltd 4 products
2 mg sublingual tabletNDC 72888-0182-30 Lactose Corn-derived Sorbitol or mannitol
Show 6 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

4 mg sublingual tabletNDC 72888-0509-01 Lactose Corn-derived Sorbitol or mannitol
Show 6 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 72888-0183-30 Lactose Corn-derived Sorbitol or mannitol
Show 6 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

12 mg sublingual tabletNDC 72888-0510-01 Lactose Corn-derived Sorbitol or mannitol
Show 6 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Alvogen Inc. 4 products
BUPRENORPHINE 5 mcg/h skin patchNDC 47781-0406-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE K90

BUPRENORPHINE 10 mcg/h skin patchNDC 47781-0407-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE K90

BUPRENORPHINE 15 mcg/h skin patchNDC 47781-0419-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE K90

BUPRENORPHINE 20 mcg/h skin patchNDC 47781-0408-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE K90

American Health Packaging 2 products
2 mg sublingual tabletNDC 60687-0481-21 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 60687-0492-21 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Amneal Pharmaceuticals NY LLC 5 products
BUPRENORPHINE 5 mcg/h skin patchNDC 69238-1202-02 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE

BUPRENORPHINE 7.5 mcg/h skin patchNDC 69238-1505-02 Still being read Not read yet
BUPRENORPHINE 10 mcg/h skin patchNDC 69238-1203-02 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE

BUPRENORPHINE 15 mcg/h skin patchNDC 69238-1204-02 Still being read Not read yet
BUPRENORPHINE 20 mcg/h skin patchNDC 69238-1205-02 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE

Aveva Drug Delivery Systems Inc. 5 products
BUPRENORPHINE 5 mcg/h skin patchNDC 03215-1521-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE, UNSPECIFIED

BUPRENORPHINE 7.5 mcg/h skin patchNDC 03215-1522-04 Still being read Not read yet
BUPRENORPHINE 10 mcg/h skin patchNDC 03215-1523-04 Still being read Not read yet
BUPRENORPHINE 15 mcg/h skin patchNDC 03215-1524-04 Still being read Not read yet
BUPRENORPHINE 20 mcg/h skin patchNDC 03215-1525-04 Still being read Not read yet
AvPAK 2 products
2 mg sublingual tabletNDC 50268-0128-15 Still being read Not read yet
8 mg sublingual tabletNDC 50268-0129-15 Still being read Not read yet
BioDelivery Sciences International Inc 7 products
75 mcg buccal filmNDC 59385-0021-60 Titanium dioxide Propylene glycol
Show 16 ingredients

.ALPHA.-TOCOPHEROL ACETATE, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 38 MPA.S AT 2%), Ferric Oxide Yellow, HYDROXYETHYL CELLULOSE (280 MPA.S AT 5%), HYDROXYPROPYL CELLULOSE (90000 WAMW), Methylparaben, Peppermint Oil, Polycarbophil, Propylene Glycol, Propylparaben, Saccharin Sodium, Sodium Benzoate, Sodium Hydroxide, SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS, Titanium Dioxide

150 mcg buccal filmNDC 59385-0022-60 Still being read Not read yet
300 mcg buccal filmNDC 59385-0023-60 Titanium dioxide Propylene glycol
Show 16 ingredients

.ALPHA.-TOCOPHEROL ACETATE, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 38 MPA.S AT 2%), Ferric Oxide Yellow, HYDROXYETHYL CELLULOSE (280 MPA.S AT 5%), HYDROXYPROPYL CELLULOSE (90000 WAMW), Methylparaben, Peppermint Oil, Polycarbophil, Propylene Glycol, Propylparaben, Saccharin Sodium, Sodium Benzoate, Sodium Hydroxide, SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS, Titanium Dioxide

450 mcg buccal filmNDC 59385-0024-60 Still being read Not read yet
600 mcg buccal filmNDC 59385-0025-60 Titanium dioxide Propylene glycol
Show 16 ingredients

.ALPHA.-TOCOPHEROL ACETATE, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 38 MPA.S AT 2%), Ferric Oxide Yellow, HYDROXYETHYL CELLULOSE (280 MPA.S AT 5%), HYDROXYPROPYL CELLULOSE (90000 WAMW), Methylparaben, Peppermint Oil, Polycarbophil, Propylene Glycol, Propylparaben, Saccharin Sodium, Sodium Benzoate, Sodium Hydroxide, SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS, Titanium Dioxide

750 mcg buccal filmNDC 59385-0026-60 Still being read Not read yet
900 mcg buccal filmNDC 59385-0027-60 Titanium dioxide Propylene glycol
Show 16 ingredients

.ALPHA.-TOCOPHEROL ACETATE, ANHYDROUS CITRIC ACID, CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 38 MPA.S AT 2%), Ferric Oxide Yellow, HYDROXYETHYL CELLULOSE (280 MPA.S AT 5%), HYDROXYPROPYL CELLULOSE (90000 WAMW), Methylparaben, Peppermint Oil, Polycarbophil, Propylene Glycol, Propylparaben, Saccharin Sodium, Sodium Benzoate, Sodium Hydroxide, SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS, Titanium Dioxide

Braeburn Inc. 7 products
8 mg/0.16 mL injectionNDC 58284-0208-01 Soy Alcohol (ethanol)
Show 3 ingredients

ALCOHOL, GLYCERYL DIOLEATE, LECITHIN, SOYBEAN

16 mg/0.32 mL injectionNDC 58284-0216-01 Still being read Not read yet
24 mg/0.48 mL injectionNDC 58284-0224-01 Still being read Not read yet
32 mg/0.64 mL injectionNDC 58284-0232-01 Soy Alcohol (ethanol)
Show 3 ingredients

ALCOHOL, GLYCERYL DIOLEATE, LECITHIN, SOYBEAN

64 mg/0.18 mL injectionNDC 58284-0264-01 Still being read Not read yet
96 mg/0.27 mL injectionNDC 58284-0296-01 Still being read Not read yet
128 mg/0.36 mL injectionNDC 58284-0228-01 Soy
Show 3 ingredients

GLYCERYL DIOLEATE, LECITHIN, SOYBEAN, METHYLPYRROLIDONE

Bryant Ranch Prepack 7 products
2 mg sublingual tabletNDC 72162-1344-03 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

2 mg sublingual tabletNDC 63629-9475-01 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

2 mg sublingual tabletNDC 71335-0950-01 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 71335-1163-00 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

8 mg sublingual tabletNDC 71335-3152-00 Still being read Not read yet
8 mg sublingual tabletNDC 72162-1345-00 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 71335-1154-00 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Camber Pharmaceuticals, Inc. 2 products
2 mg sublingual tabletNDC 31722-0870-30 Lactose Corn-derived Sorbitol or mannitol
Show 11 ingredients

ACESULFAME POTASSIUM, ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

8 mg sublingual tabletNDC 31722-0871-30 Lactose Corn-derived Sorbitol or mannitol
Show 11 ingredients

ACESULFAME POTASSIUM, ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

Clinical Solutions Wholesale, LLC 6 products
2 mg sublingual tabletNDC 58118-0176-08 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (15 MPA.S AT 5%), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

2 mg sublingual tabletNDC 58118-0501-08 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

2 mg sublingual tabletNDC 58118-4459-08 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN

8 mg sublingual tabletNDC 58118-0177-08 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (15 MPA.S AT 5%), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

8 mg sublingual tabletNDC 58118-0460-08 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN

8 mg sublingual tabletNDC 58118-0502-08 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Direct_Rx 2 products
2 mg sublingual tabletNDC 72189-0580-60 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

8 mg sublingual tabletNDC 72189-0582-60 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

Direct_rx 1 product
2 mg sublingual tabletNDC 72189-0579-60 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN

Hikma Pharmaceuticals USA Inc. 3 products
0.324 mg/mL injectionNDC 00143-9246-05 Sugar (sucrose, dextrose)
Show 3 ingredients

ANHYDROUS DEXTROSE, HYDROCHLORIC ACID, WATER

2 mg sublingual tabletNDC 00054-0176-13 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

8 mg sublingual tabletNDC 00054-0177-13 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

Hospira, Inc. 1 product
0.3 mg/mL injectionNDC 00409-2012-32 Sugar (sucrose, dextrose)
Show 3 ingredients

ANHYDROUS DEXTROSE, HYDROCHLORIC ACID, WATER

Indivior Inc. 2 products
100 mg injectionNDC 12496-0100-01 None of these listed
Show 2 ingredients

METHYLPYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 15000 MW)

300 mg injectionNDC 12496-0300-01 None of these listed
Show 2 ingredients

METHYLPYRROLIDONE, POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 15000 MW)

Ingenus Pharmaceuticals, Llc 5 products
BUPRENORPHINE 5 mcg/h skin patchNDC 50742-0372-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE, UNSPECIFIED

BUPRENORPHINE 7.5 mcg/h skin patchNDC 50742-0373-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE, UNSPECIFIED

BUPRENORPHINE 10 mcg/h skin patchNDC 50742-0374-04 Still being read Not read yet
BUPRENORPHINE 15 mcg/h skin patchNDC 50742-0375-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE, UNSPECIFIED

BUPRENORPHINE 20 mcg/h skin patchNDC 50742-0376-04 None of these listed
Show 3 ingredients

LEVULINIC ACID, OLEYL OLEATE, POVIDONE, UNSPECIFIED

Knoa Pharma LLC 5 products
BUPRENORPHINE 5 mcg/h skin patchNDC 59011-0750-04 None of these listed
Show 3 ingredients

ETHYL LEVULINATE, OLEYL OLEATE, POVIDONE, UNSPECIFIED

BUPRENORPHINE 7.5 mcg/h skin patchNDC 59011-0757-04 None of these listed
Show 3 ingredients

ETHYL LEVULINATE, OLEYL OLEATE, POVIDONE, UNSPECIFIED

BUPRENORPHINE 10 mcg/h skin patchNDC 59011-0751-04 Still being read Not read yet
BUPRENORPHINE 15 mcg/h skin patchNDC 59011-0758-04 Still being read Not read yet
BUPRENORPHINE 20 mcg/h skin patchNDC 59011-0752-04 None of these listed
Show 3 ingredients

ETHYL LEVULINATE, OLEYL OLEATE, POVIDONE, UNSPECIFIED

LTS Therapy Systems, LLC 1 product
BUPRENORPHINE 20 mcg/h skin patchNDC 58064-0408-04 No current label Not available
Major Pharmaceuticals 2 products
2 mg sublingual tabletNDC 00904-7154-04 Still being read Not read yet
8 mg sublingual tabletNDC 00904-7155-04 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

PAI Holdings, LLC dba PAI Pharma 2 products
2 mg sublingual tabletNDC 00121-1019-30 Lactose Corn-derived Sorbitol or mannitol
Show 7 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MANNITOL, POVIDONE K30, SODIUM STEARYL FUMARATE, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 00121-2038-30 Lactose Corn-derived Sorbitol or mannitol
Show 7 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MANNITOL, POVIDONE K30, SODIUM STEARYL FUMARATE, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Par Health USA, LLC 1 product
0.324 mg/mL injectionNDC 42023-0179-05 Sugar (sucrose, dextrose)
Show 3 ingredients

ANHYDROUS DEXTROSE, HYDROCHLORIC ACID, WATER

Redpharm Drug 2 products
2 mg sublingual tabletNDC 67296-2123-03 Still being read Not read yet
8 mg sublingual tabletNDC 67296-2173-03 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN

Remedyrepack Inc. 5 products
2 mg sublingual tabletNDC 70518-1557-01 Lactose Corn-derived Synthetic dyes Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (15 MPA.S AT 5%), FD&C YELLOW NO. 6, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

2 mg sublingual tabletNDC 70518-2226-00 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

2 mg sublingual tabletNDC 70518-4570-00 Lactose Corn-derived Sorbitol or mannitol
Show 6 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 70518-2014-00 Lactose Corn-derived Sorbitol or mannitol
Show 9 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE (120 .MU.M), LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN, WATER

8 mg sublingual tabletNDC 70518-4571-00 Lactose Corn-derived Sorbitol or mannitol
Show 7 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MANNITOL, POVIDONE K30, SODIUM STEARYL FUMARATE, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

Rhodes Pharmaceuticals LLC 7 products
BUPRENORPHINE 5 mcg/h skin patchNDC 42858-0750-40 None of these listed
Show 3 ingredients

ethyl levulinate, oleyl oleate, povidone, unspecified

BUPRENORPHINE 7.5 mcg/h skin patchNDC 42858-0353-40 None of these listed
Show 3 ingredients

ethyl levulinate, oleyl oleate, povidone, unspecified

BUPRENORPHINE 10 mcg/h skin patchNDC 42858-0493-40 None of these listed
Show 3 ingredients

ethyl levulinate, oleyl oleate, povidone, unspecified

BUPRENORPHINE 15 mcg/h skin patchNDC 42858-0586-40 None of these listed
Show 3 ingredients

ethyl levulinate, oleyl oleate, povidone, unspecified

BUPRENORPHINE 20 mcg/h skin patchNDC 42858-0839-40 None of these listed
Show 3 ingredients

ethyl levulinate, oleyl oleate, povidone, unspecified

2 mg sublingual tabletNDC 42858-0501-03 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

Anhydrous Citric Acid, CROSPOVIDONE, UNSPECIFIED, Lactose monohydrate, Magnesium Stearate, Mannitol, Povidone K30, Starch, Corn, Trisodium Citrate Dihydrate

8 mg sublingual tabletNDC 42858-0502-03 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

Anhydrous Citric Acid, CROSPOVIDONE, UNSPECIFIED, Lactose monohydrate, Magnesium Stearate, Mannitol, Povidone K30, Starch, Corn, Trisodium Citrate Dihydrate

Somerset Therapeutics, LLC 1 product
0.324 mg/mL injectionNDC 70069-0027-05 Sugar (sucrose, dextrose)
Show 3 ingredients

ANHYDROUS DEXTROSE, HYDROCHLORIC ACID, WATER

SpecGx LLC 2 products
2 mg sublingual tabletNDC 00406-7012-03 Lactose Corn-derived Sorbitol or mannitol
Show 7 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MANNITOL, POVIDONE, SODIUM CITRATE, SODIUM STEARYL FUMARATE, STARCH, CORN

8 mg sublingual tabletNDC 00406-7018-03 Lactose Corn-derived Sorbitol or mannitol
Show 7 ingredients

ANHYDROUS CITRIC ACID, LACTOSE MONOHYDRATE, MANNITOL, POVIDONE, SODIUM CITRATE, SODIUM STEARYL FUMARATE, STARCH, CORN

Sun Pharmaceutical Industries, Inc. 2 products
2 mg sublingual tabletNDC 62756-0459-64 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN

8 mg sublingual tabletNDC 62756-0460-64 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, BUTYLATED HYDROXYANISOLE, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE, UNSPECIFIED, SODIUM CITRATE, UNSPECIFIED FORM, STARCH, CORN

Teva Pharmaceuticals USA, Inc. 5 products
BUPRENORPHINE 5 mcg/h skin patchNDC 00093-3656-40 None of these listed
Show 2 ingredients

CITRIC ACID MONOHYDRATE, LEVULINIC ACID

BUPRENORPHINE 7.5 mcg/h skin patchNDC 00093-3239-40 None of these listed
Show 2 ingredients

CITRIC ACID MONOHYDRATE, LEVULINIC ACID

BUPRENORPHINE 10 mcg/h skin patchNDC 00093-3657-40 None of these listed
Show 2 ingredients

CITRIC ACID MONOHYDRATE, LEVULINIC ACID

BUPRENORPHINE 15 mcg/h skin patchNDC 00093-3658-40 Still being read Not read yet
BUPRENORPHINE 20 mcg/h skin patchNDC 00093-3659-40 None of these listed
Show 2 ingredients

CITRIC ACID MONOHYDRATE, LEVULINIC ACID

Unit Dose Solutions, Inc. 2 products
2 mg sublingual tabletNDC 87441-0011-01 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

8 mg sublingual tabletNDC 87441-0082-01 Lactose Corn-derived Sorbitol or mannitol
Show 8 ingredients

ANHYDROUS CITRIC ACID, CROSPOVIDONE, UNSPECIFIED, LACTOSE MONOHYDRATE, MAGNESIUM STEARATE, MANNITOL, POVIDONE K30, STARCH, CORN, TRISODIUM CITRATE DIHYDRATE

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.

Buprenorphine without lactose

Lactose: milk sugar; a concern with lactose intolerance or a milk allergy. 46 of 83 checked products list lactose; 37 do not.

Lists lactose

Buprenorphine without soy

Soy: soybean oil or soy lecithin; a concern with soy allergy. 3 of 83 checked products list soy; 80 do not.

Does not list soy

Buprenorphine without synthetic dyes

Synthetic dyes: FD&C or D&C colorants and their aluminum lakes. 3 of 83 checked products list synthetic dyes; 80 do not.

Does not list synthetic dyes

Lists synthetic dyes

Buprenorphine without corn-derived ingredients

Corn-derived: corn starch, maize or corn syrup; a concern with corn allergy. 46 of 83 checked products list corn-derived ingredients; 37 do not.

Lists corn-derived ingredients

Buprenorphine without titanium dioxide

Titanium dioxide: A white colorant some people choose to avoid. 4 of 83 checked products list titanium dioxide; 79 do not.

Does not list titanium dioxide

Lists titanium dioxide

Buprenorphine without alcohol (ethanol)

Alcohol (ethanol): mostly in liquids; a concern in alcohol recovery, for children, or with disulfiram or metronidazole. 2 of 83 checked products list alcohol (ethanol); 81 do not.

Does not list alcohol (ethanol)

Lists alcohol (ethanol)

Buprenorphine without propylene glycol

Propylene glycol: A solvent in liquids and capsules; a concern in kidney disease, for infants, and at high doses. 4 of 83 checked products list propylene glycol; 79 do not.

Does not list propylene glycol

Lists propylene glycol

Buprenorphine without sorbitol or mannitol

Sorbitol or mannitol: sugar alcohols that can cause bloating or diarrhea in larger amounts. 46 of 83 checked products list sorbitol or mannitol; 37 do not.

Lists sorbitol or mannitol

Buprenorphine without sugar (sucrose or dextrose)

Sugar (sucrose, dextrose): A consideration in diabetes, mostly in liquids and chewables. 4 of 83 checked products list sugar (sucrose or dextrose); 79 do not.

Does not list sugar (sucrose or dextrose)

Lists sugar (sucrose or dextrose)

At the pharmacy counter

How to use this at the pharmacy counter

  1. 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.
  2. 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.
  3. 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.
  4. 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.
Ask Dr. Staiger which Buprenorphine product suits you →

Common questions about Buprenorphine inactive ingredients

Is Buprenorphine gluten-free?
This page cannot certify any Buprenorphine product gluten-free; it reports what each label declares. Of the 83 products checked, none lists a wheat, barley, rye or gluten ingredient, and none lists a starch without a stated source. If you have celiac disease, ask the manufacturer's medical information line for a written gluten statement for the lot you have.
Does Buprenorphine contain lactose?
46 of 83 checked Buprenorphine products list lactose; 37 do not: Alvogen (BUPRENORPHINE 5 mcg/h skin patch, BUPRENORPHINE 10 mcg/h skin patch and BUPRENORPHINE 15 mcg/h skin patch and 1 more), Amneal (BUPRENORPHINE 5 mcg/h skin patch, BUPRENORPHINE 10 mcg/h skin patch and BUPRENORPHINE 20 mcg/h skin patch), Aveva Drug Delivery Systems (BUPRENORPHINE 5 mcg/h skin patch) and BioDelivery Sciences (75 mcg buccal film, 300 mcg buccal film and 600 mcg buccal film and 1 more) and 10 other companies. The lactose in a tablet or capsule is a small amount, but people with a milk allergy or a strong intolerance often prefer a version that does not list it.
Does Buprenorphine contain soy?
3 of 83 checked Buprenorphine products list a soy ingredient (soybean oil or soy lecithin); 80 do not: A-S Medication Solutions (8 mg sublingual tablet), Actavis (2 mg sublingual tablet and 8 mg sublingual tablet), Advagen (2 mg sublingual tablet, 4 mg sublingual tablet and 8 mg sublingual tablet and 1 more) and Alvogen (BUPRENORPHINE 5 mcg/h skin patch, BUPRENORPHINE 10 mcg/h skin patch and BUPRENORPHINE 15 mcg/h skin patch and 1 more) and 25 other companies. Soy lecithin is the usual form and the amount is small, but people with a soy allergy often prefer a version that does not list it.
Is there a dye-free Buprenorphine?
3 of 83 checked Buprenorphine products list a synthetic dye (an FD&C or D&C colorant); 80 do not: A-S Medication Solutions (8 mg sublingual tablet), Advagen (2 mg sublingual tablet, 4 mg sublingual tablet and 8 mg sublingual tablet and 1 more), Alvogen (BUPRENORPHINE 5 mcg/h skin patch, BUPRENORPHINE 10 mcg/h skin patch and BUPRENORPHINE 15 mcg/h skin patch and 1 more) and American Health Packaging (2 mg sublingual tablet and 8 mg sublingual tablet) and 25 other companies. Colorants often differ by strength within one company's line, so compare the lists above strength by strength.
Does Buprenorphine contain gelatin?
No checked Buprenorphine product lists gelatin on its label. Gelatin is usually bovine or porcine and the label rarely says which; for kosher, halal or vegetarian needs, ask the manufacturer.
Why do the inactive ingredients differ between manufacturers?
A generic must match the brand's active ingredient, strength, dose form and how it is absorbed; its fillers, binders, coatings and colorants are the manufacturer's own choice. That is why one Buprenorphine product can list lactose and a dye while another from a different company lists neither.
Can my pharmacy give me a specific manufacturer's version?
Often, if you ask before the prescription is filled: many pharmacies order from wholesalers that carry several companies' versions and can request a particular one. Some pharmacies buy a generic from one contracted source only, and a few insurance plans cover only certain NDCs, so ask the pharmacist to check. Give them the NDC from this page; the company name alone is often enough.
How current is this list?
The products are the ones in the FDA's current NDC directory as of October 5, 2026, and each inactive-ingredient list is the manufacturer's FDA label as our label sync last read it. Formulations change, so check the label on your own bottle and ask your pharmacist if a refill looks different.

Sources: the products are the finished Buprenorphine 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 Buprenorphine guide