Pill Identifier Divalproex Sodium - NDC 68788-7177
Divalproex Sodium
Product Code 68788-7177
Divalproex Sodium by Preferred Pharmaceuticals Inc. is a gray oval tablet film coated extended release about 19 mm in size, imprinted with i50. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- FD&C BLUE NO. 1
- FD&C BLUE NO. 2
- HYPROMELLOSE 2208 (100 MPA.S)
- HYPROMELLOSE 2910 (3 MPA.S)
- HYPROMELLOSE 2910 (6 MPA.S)
- MANNITOL
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYETHYLENE GLYCOL 8000
- STARCH, CORN
- PROPYLENE GLYCOL
- SHELLAC
- MICROCRYSTALLINE CELLULOSE
- SILICON DIOXIDE
- TITANIUM DIOXIDE
- TRIACETIN
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- POLYDEXTROSE
Preferred Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated, Extended Release
- Gray (C48324)
Product Packages
NDC Package Code | Package Description |
---|---|
68788-7177-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
68788-7177-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
68788-7177-9 | 90 TABLET, FILM COATED, EXTENDED 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.