Pill Identifier Divalproex Sodium - NDC 67046-150
Product Code 67046-150
Divalproex Sodium by Contract Pharmacy Services-pa is a white capsule about 21 mm in size, imprinted with an;757. The product is a with active ingredient(s) .
Divalproex Sodium
Active Ingredient(s):
Inactive Ingredient(s):
- AMMONIA
- ETHYL ACRYLATE
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
- HYPROMELLOSES
- FERROSOFERRIC OXIDE
- ISOPROPYL ALCOHOL
- LACTOSE MONOHYDRATE
- POLYETHYLENE GLYCOLS
- MAGNESIUM STEARATE
- CELLULOSE, MICROCRYSTALLINE
- BUTYL ALCOHOL
- POLYVINYL ALCOHOL, UNSPECIFIED
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- TALC
- TITANIUM DIOXIDE
Contract Pharmacy Services-pa
Product Type:
Dosage Form:
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
67046-150-07 | 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-14 | 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-15 | 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-20 | 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-21 | 21 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-28 | 28 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-30 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
67046-150-60 | 60 TABLET, EXTENDED 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.