Pill Identifier Divalproex Sodium Delayed Release - NDC 49349-072
Product Code 49349-072
Divalproex Sodium Delayed Release by Remedyrepack Inc. is a pink oval about 19 mm in size, imprinted with 93;7441. The product is a with active ingredient(s) .
Divalproex Sodium Delayed Release
Active Ingredient(s):
Inactive Ingredient(s):
- CROSPOVIDONE
- HYPROMELLOSE 2208 (100 MPA.S)
- FERROSOFERRIC OXIDE
- LACTOSE MONOHYDRATE
- MAGNESIUM STEARATE
- CELLULOSE, MICROCRYSTALLINE
- ISOBUTYL ALCOHOL
- PEG-12 LAURATE
- POLYVINYL ALCOHOL
- POVIDONE
- STARCH, CORN
- SILICON DIOXIDE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- PHENOXYISOPROPANOL
- LECITHIN, SOYBEAN
- FERRIC OXIDE RED
- FERRIC OXIDE YELLOW
- TRIACETIN
Remedyrepack Inc.
Product Type:
Dosage Form:
- Pink (C48328)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 49349-072-02 | 30 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.