Pill Identifier Divalproex Sodium - NDC 68180-260
Divalproex Sodium
Product Code 68180-260
Divalproex Sodium by Lupin Pharmaceuticals, Inc. is a white oval tablet extended release about 14 mm in size, imprinted with l088. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- ETHYL ACRYLATE AND METHYL METHACRYLATE COPOLYMER (2:1
- 750000 MW)
- ETHYLCELLULOSE (7 MPA.S)
- FERROSOFERRIC OXIDE
- HYPROMELLOSE 2208 (100000 MPA.S)
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- POLYETHYLENE GLYCOL 3350
- POLYETHYLENE GLYCOL 6000
- POLYVINYL ALCOHOL, UNSPECIFIED
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- TALC
- TITANIUM DIOXIDE
Lupin Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68180-260-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68180-260-02 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE |
68180-260-06 | 30 TABLET, 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.