Pill Identifier Zolpidem Tartrate - NDC 61919-449
Zolpidem Tartrate
Product Code 61919-449
Zolpidem Tartrate by Direct Rx is a yellow rou tablet film coated extended release about 8 mm in size, imprinted with a1. The product is a human prescription drug with active ingredient(s) zolpidem tartrate.
Zolpidem Tartrate
Active Ingredient(s): Zolpidem Tartrate
Inactive Ingredient(s):
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE, UNSPECIFIED
- POLYDEXTROSE
- HYPROMELLOSE 2910 (5 MPA.S)
- MAGNESIUM STEARATE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- TITANIUM DIOXIDE
- ANHYDROUS LACTOSE
- SILICON DIOXIDE
- HYPROMELLOSE 2208 (4000 MPA.S)
- MICROCRYSTALLINE CELLULOSE
- TALC
- TRIETHYL CITRATE
- TRIACETIN
- SODIUM BICARBONATE
- SODIUM LAURYL SULFATE
- TARTARIC ACID
- FERRIC OXIDE YELLOW
Direct Rx
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Yellow (C48330)
DEA Schedule: CIV
Product Packages
NDC Package Code | Package Description |
---|---|
61919-449-30 | 30 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.