Pill Identifier Minocycline - NDC 57664-856
Minocycline Hydrochloride
Product Code 57664-856
Minocycline by Sun Pharmaceutical Industries, Inc. is a gray capsule tablet film coated about 13 mm in size, imprinted with 856. The product is a human prescription drug with active ingredient(s) minocycline hydrochloride.
Minocycline
Active Ingredient(s): Minocycline Hydrochloride
Inactive Ingredient(s):
- LACTOSE MONOHYDRATE
- MICROCRYSTALLINE CELLULOSE
- POVIDONE, UNSPECIFIED
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- SILICON DIOXIDE
- MAGNESIUM STEARATE
- HYPROMELLOSE, UNSPECIFIED
- TITANIUM DIOXIDE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- FERROSOFERRIC OXIDE
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Gray (C48324)
Product Packages
NDC Package Code | Package Description |
---|---|
57664-856-13 | 500 TABLET, FILM COATED in 1 BOTTLE |
57664-856-18 | 1000 TABLET, FILM COATED in 1 BOTTLE |
57664-856-85 | 50 TABLET, FILM COATED in 1 BOTTLE |
57664-856-88 | 100 TABLET, FILM COATED 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.