Pill Identifier Zolpidem Tartrate - NDC 47335-307
Zolpidem Tartrate
Product Code 47335-307
Zolpidem Tartrate by Sun Pharmaceutical Industries, Inc. is a pink and white rou tablet film coated extended release about 8 mm in size, imprinted with 307. The product is a human prescription drug with active ingredient(s) zolpidem tartrate.
Zolpidem Tartrate
Active Ingredient(s): Zolpidem Tartrate
Inactive Ingredient(s):
- LACTOSE MONOHYDRATE
- MICROCRYSTALLINE CELLULOSE
- FERRIC OXIDE RED
- HYPROMELLOSE, UNSPECIFIED
- SODIUM STARCH GLYCOLATE TYPE A POTATO
- MAGNESIUM STEARATE
- TARTARIC ACID
- SHELLAC
- PROPYLENE GLYCOL
- BUTYL ALCOHOL
- FERROSOFERRIC OXIDE
- AMMONIA
- TALC
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYSORBATE 80
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Pink (C48328)
- White (C48325)
DEA Schedule: CIV
Product Packages
NDC Package Code | Package Description |
---|---|
47335-307-13 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
47335-307-88 | 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.