Pill Identifier Bupropion Hydrochloride - NDC 69844-010
Bupropion Hydrochloride
Product Code 69844-010
Bupropion Hydrochloride by Graviti Pharmaceuticals Private Limited is a white rou tablet extended release about 9 mm in size, imprinted with 189. The product is a human prescription drug with active ingredient(s) bupropion hydrochloride.
Bupropion Hydrochloride
Active Ingredient(s): Bupropion Hydrochloride
Inactive Ingredient(s):
- ETHYLCELLULOSE (100 MPA.S)
- GLYCERYL DIBEHENATE
- HYDROCHLORIC ACID
- MAGNESIUM STEARATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- METHYLENE CHLORIDE
- POLYETHYLENE GLYCOL 1450
- POVIDONE K90
- SILICON DIOXIDE
- TRIETHYL CITRATE
- HYPROMELLOSE, UNSPECIFIED
- TRICETIN
- TALC
- SHELLAC
- FERROSOFERRIC OXIDE
- PROPYLENE GLYCOL
- AMMONIA
Graviti Pharmaceuticals Private Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
69844-010-01 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE |
69844-010-02 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE |
69844-010-03 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE |
* 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.