Pill Identifier Divalproex Sodium - NDC 65862-403
Divalproex Sodium
Product Code 65862-403
Divalproex Sodium by Aurobindo Pharma Limited is a pink oval tablet delayed release about 19 mm in size, imprinted with d;86. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- SILICON DIOXIDE
- MICROCRYSTALLINE CELLULOSE
- CROSCARMELLOSE SODIUM
- POVIDONE K30
- LOW-SUBSTITUTED HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- TALC
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- DIETHYL PHTHALATE
- HYPROMELLOSE 2910 (15 MPA.S)
- TRIACETIN
- POLYVINYL ALCOHOL, UNSPECIFIED
- TITANIUM DIOXIDE
- POLYETHYLENE GLYCOL 3350
- LECITHIN, SOYBEAN
- FD&C RED NO. 40
- VANILLIN
- FD&C BLUE NO. 2
- SHELLAC
- ISOPROPYL ALCOHOL
- FERROSOFERRIC OXIDE
- BUTYL ALCOHOL
- PROPYLENE GLYCOL
- AMMONIA
Aurobindo Pharma Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
65862-403-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE |
65862-403-05 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE |
65862-403-10 | 10 BLISTER PACK in 1 CARTON > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
65862-403-22 | 2000 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.