Pill Identifier Metformin Hydrochloride - NDC 47335-305
Metformin Hydrochloride
Product Code 47335-305
Metformin Hydrochloride by Sun Pharmaceutical Industries, Inc. is a white rou tablet film coated extended release about 11 mm in size, imprinted with 305. The product is a human prescription drug with active ingredient(s) metformin hydrochloride.
Metformin Hydrochloride
Active Ingredient(s): Metformin Hydrochloride
Inactive Ingredient(s):
- SODIUM LAURYL SULFATE
- POVIDONE, UNSPECIFIED
- ANHYDROUS CITRIC ACID
- SODIUM BICARBONATE
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- ETHYLCELLULOSE (100 MPA.S)
- DIBUTYL SEBACATE
- AMMONIA
- FERROSOFERRIC OXIDE
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- SHELLAC
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
47335-305-18 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
47335-305-83 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
47335-305-88 | 100 TABLET, FILM COATED, 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.