Pill Identifier Bupropion Hydrochloride XL - NDC 0591-3331
Bupropion Hydrochloride
Product Code 0591-3331
Bupropion Hydrochloride XL by Actavis Pharma, Inc. is a white rou tablet film coated extended release about 8 mm in size, imprinted with wpi;3331. The product is a human prescription drug with active ingredient(s) bupropion hydrochloride.
Bupropion Hydrochloride XL
Active Ingredient(s): Bupropion Hydrochloride
Inactive Ingredient(s):
- SILICON DIOXIDE
- ETHYLCELLULOSES
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- CELLULOSE, MICROCRYSTALLINE
- STEARIC ACID
- TALC
- TITANIUM DIOXIDE
- HYDROCHLORIC ACID
- TRIETHYL CITRATE
Actavis Pharma, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
0591-3331-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
0591-3331-19 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
0591-3331-30 | 30 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.