Pill Identifier Divalproex Sodium - NDC 0904-6861
Divalproex Sodium
Product Code 0904-6861
Divalproex Sodium by Major Pharmaceuticals is a pink oval tablet delayed release about 19 mm in size, imprinted with 798. 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
- D&C RED NO. 30
- FD&C BLUE NO. 2
- SHELLAC
- FERROSOFERRIC OXIDE
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- AMMONIA
- FERRIC OXIDE RED
- TALC
Major Pharmaceuticals
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
0904-6861-61 | 100 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
0904-6861-90 | 90 BLISTER PACK in 1 CARTON > 1 TABLET, DELAYED RELEASE 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.