Pill Identifier Divalproex Sodium - NDC 55111-529
Divalproex Sodium
Product Code 55111-529
Divalproex Sodium by Dr.reddy's Laboratories Limited is a brow capsule tablet delayed release about 12 mm in size, imprinted with r529. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- acetone
- diacetylated monoglycerides
- hypromelloses
- isopropyl alcohol
- methylene chloride
- cellulose, microcrystalline
- povidone
- starch, corn
- silicon dioxide
- talc
- titanium dioxide
- vanillin
- shellac
- Ferrosoferric Oxide
- brown iron oxide
- butyl alcohol
- lecithin, soybean
Dr.reddy's Laboratories Limited
Product Type: Human Prescription Drug
Dosage Form: Tablet, Delayed Release
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
55111-529-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE |
55111-529-05 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE |
55111-529-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
55111-529-78 | 10 BLISTER PACK in 1 CARTON > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-529-79) |
* 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.