Pill Identifier Divalproex Sodium - NDC 68382-106
Divalproex Sodium
Product Code 68382-106
Divalproex Sodium by Zydus Pharmaceuticals (usa) Inc. is a blue and white capsule capsule coated pellets about 22 mm in size, imprinted with za66;125mg. The product is a human prescription drug with active ingredient(s) divalproex sodium.
Divalproex Sodium
Active Ingredient(s): Divalproex Sodium
Inactive Ingredient(s):
- ALCOHOL
- AMMONIA
- BUTYL ALCOHOL
- CELLULOSE, MICROCRYSTALLINE
- FD&C BLUE NO. 1
- FERROSOFERRIC OXIDE
- GELATIN
- HYPROMELLOSES
- ISOPROPYL ALCOHOL
- METHACRYLIC ACID
- POTASSIUM HYDROXIDE
- PROPYLENE GLYCOL
- SHELLAC
- SILICON DIOXIDE
- SODIUM LAURYL SULFATE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
- WATER
Zydus Pharmaceuticals (usa) Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Coated Pellets
- Blue (C48333)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68382-106-01 | 100 CAPSULE, COATED PELLETS in 1 BOTTLE |
68382-106-10 | 1000 CAPSULE, COATED PELLETS in 1 BOTTLE |
68382-106-77 | 100 BLISTER PACK in 1 CARTON > 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-106-30) |
* 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.