Pill Identifier Divalproex Sodium - NDC 68180-267
Divalproex Sodium
Product Code 68180-267
Divalproex Sodium by Lupin Pharmaceuticals, Inc. is a pink oval tablet delayed release about 19 mm in size, imprinted with l007. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- D&C RED NO. 30
- FD&C BLUE NO. 2
- FERRIC OXIDE YELLOW
- HYPROMELLOSES
- SILICON DIOXIDE
- TRIETHYL CITRATE
- CELLULOSE, MICROCRYSTALLINE
- HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST)
- HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED
- SHELLAC
- TALC
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- MAGNESIUM STEARATE
- PROPYLENE GLYCOL
- TITANIUM DIOXIDE
- FERROSOFERRIC OXIDE
- STARCH, CORN
Lupin Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
68180-267-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE |
68180-267-02 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE |
68180-267-03 | 1000 TABLET, DELAYED RELEASE in 1 BOTTLE |
68180-267-11 | 10 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.