Pill Identifier Omeprazole - NDC 68382-411
Omeprazole
Product Code 68382-411
Omeprazole by Zydus Pharmaceuticals (usa) Inc. is a purple and white capsule capsule delayed release about 10 mm in size, imprinted with za;09;10mg. The product is a human prescription drug with active ingredient(s) omeprazole.
Omeprazole
Active Ingredient(s): Omeprazole
Inactive Ingredient(s):
- ACETONE
- FD&C BLUE NO. 1
- FD&C GREEN NO. 3
- FD&C RED NO. 3
- FERROSOFERRIC OXIDE
- GELATIN
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- HYPROMELLOSE PHTHALATE (31% PHTHALATE, 170 CST)
- HYPROMELLOSES
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POTASSIUM HYDROXIDE
- PROPYLENE GLYCOL
- SHELLAC
- SODIUM LAURYL SULFATE
- SODIUM PHOSPHATE, DIBASIC, DIHYDRATE
- SUCROSE
- TALC
- TITANIUM DIOXIDE
- TRIETHYL CITRATE
Zydus Pharmaceuticals (usa) Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release
- Purple (C48327)
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
68382-411-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
68382-411-05 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
68382-411-06 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
68382-411-10 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
68382-411-16 | 90 CAPSULE, 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.