Pill Identifier Nateglinide - NDC 68382-721
Nateglinide
Product Code 68382-721
Nateglinide by Zydus Pharmaceuticals (usa) Inc. is a white rou tablet film coated about 10 mm in size, imprinted with 721. The product is a human prescription drug with active ingredient(s) nateglinide.
Nateglinide
Active Ingredient(s): Nateglinide
Inactive Ingredient(s):
- ANHYDROUS CITRIC ACID
- SILICON DIOXIDE
- STARCH, CORN
- HYPROMELLOSES
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- POLYSORBATE 80
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE
- TALC
- TITANIUM DIOXIDE
- CROSPOVIDONE, UNSPECIFIED
Zydus Pharmaceuticals (usa) Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68382-721-01 | 100 TABLET, FILM COATED in 1 BOTTLE |
68382-721-05 | 500 TABLET, FILM COATED in 1 BOTTLE |
68382-721-06 | 30 TABLET, FILM COATED in 1 BOTTLE |
68382-721-10 | 1000 TABLET, FILM COATED in 1 BOTTLE |
68382-721-16 | 90 TABLET, FILM COATED in 1 BOTTLE |
68382-721-77 | 10 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED in 1 BLISTER PACK |
* 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.