Pill Identifier Divalproex Sodium - NDC 68382-133
Divalproex Sodium
Product Code 68382-133
Divalproex Sodium by Zydus Pharmaceuticals (usa) Inc. is a white capsule tablet film coated extended release about 18 mm in size, imprinted with za47. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- AMMONIA
- BUTYL ALCOHOL
- FERROSOFERRIC OXIDE
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- HYPROMELLOSES
- ISOPROPYL ALCOHOL
- LECITHIN, SOYBEAN
- MAGNESIUM STEARATE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYVINYL ALCOHOL, UNSPECIFIED
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- TALC
- TITANIUM DIOXIDE
- XANTHAN GUM
Zydus Pharmaceuticals (usa) Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68382-133-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
68382-133-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
68382-133-14 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
68382-133-16 | 90 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.