Pill Identifier Divalproex Sodium - NDC 62756-796
Divalproex Sodium
Product Code 62756-796
Divalproex Sodium by Sun Pharmaceutical Industries, Inc. is a pink oval tablet delayed release about 12 mm in size, imprinted with 796. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- SILICON DIOXIDE
- STARCH, CORN
- POVIDONE, UNSPECIFIED
- HYPROMELLOSE, UNSPECIFIED
- TITANIUM DIOXIDE
- TRIACETIN
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- TRIETHYL CITRATE
- SODIUM BICARBONATE
- SODIUM LAURYL SULFATE
- FD&C RED NO. 40
- FD&C BLUE NO. 2
- SHELLAC
- FERROSOFERRIC OXIDE
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- AMMONIA
- TALC
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
62756-796-08 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE |
62756-796-13 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE |
62756-796-18 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE |
62756-796-83 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
62756-796-88 | 100 TABLET, DELAYED 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.