Pill Identifier Divalproex Sodium ER - NDC 64679-724
Divalproex Sodium
Product Code 64679-724
Divalproex Sodium ER by Wockhardt Usa Llc. is a white oval tablet film coated extended release about 15 mm in size, imprinted with w;724. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium ER
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- GLYCERYL DIBEHENATE
- HYPROMELLOSE 2910 (6 MPA.S)
- LECITHIN, SOYBEAN
- POLYETHYLENE GLYCOL 400
- POLYVINYL ALCOHOL, UNSPECIFIED
- SILICON DIOXIDE
- TALC
- TITANIUM DIOXIDE
- XANTHAN GUM
Wockhardt Usa Llc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
64679-724-01 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
64679-724-02 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
64679-724-03 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
64679-724-04 | 10 BLISTER PACK in 1 CARTON > 10 TABLET, FILM COATED, 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.