Pill Identifier Bupropion Hydrochloride SR - NDC 50228-175
Bupropion Hydrochloride
Product Code 50228-175
Bupropion Hydrochloride SR by Sciegen Pharmaceuticals, Inc. is a purple rou tablet film coated extended release about 11 mm in size, imprinted with sg;175. The product is a human prescription drug with active ingredient(s) bupropion hydrochloride.
Bupropion Hydrochloride SR
Active Ingredient(s): Bupropion Hydrochloride
Inactive Ingredient(s):
- COPOVIDONE K25-31
- CYSTEINE HYDROCHLORIDE
- HYPROMELLOSE, UNSPECIFIED
- MAGNESIUM STEARATE
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYSORBATE 80
- TITANIUM DIOXIDE
- FD&C BLUE NO. 2
- FD&C RED NO. 40
- DEXTROSE, UNSPECIFIED FORM
- ALCOHOL
- ACACIA
- PROPYLENE GLYCOL
- SILICON DIOXIDE
Sciegen Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Purple (C48327)
Product Packages
NDC Package Code | Package Description |
---|---|
50228-175-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
50228-175-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
50228-175-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
50228-175-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
50228-175-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.