Pill Identifier Divalproex Sodium - NDC 68071-4102
Divalproex Sodium
Product Code 68071-4102
Divalproex Sodium by Nucare Pharmaceuticals,inc. is a pink oval tablet delayed release about 14 mm in size, imprinted with ul;250. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- ALCOHOL
- BUTYL ALCOHOL
- CELLULOSE, MICROCRYSTALLINE
- D&C RED NO. 30
- FD&C BLUE NO. 2
- FERRIC OXIDE RED
- FERROSOFERRIC OXIDE
- HYPROMELLOSE 2910 (6 MPA.S)
- ISOPROPYL ALCOHOL
- LACTOSE MONOHYDRATE
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYETHYLENE GLYCOL 3000
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- SODIUM BICARBONATE
- SODIUM LAURYL SULFATE
- STARCH, PREGELATINIZED CORN
- TALC
- TITANIUM DIOXIDE
- TRIACETIN
- TRIETHYL CITRATE
- VANILLIN
Nucare Pharmaceuticals,inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
68071-4102-3 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
68071-4102-5 | 45 TABLET, DELAYED RELEASE in 1 BOTTLE |
68071-4102-6 | 60 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.