Omeprazole - 64861-303-01 - (Omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 64861-303
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole

Product NDC: 64861-303
Labeler Name: Dexcel Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA022032
Marketing Category: NDA
Start Marketing Date: 20080301

Package Information of Omeprazole

Package NDC: 64861-303-01
Package Description: 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64861-303-01)

NDC Information of Omeprazole

NDC Code 64861-303-01
Proprietary Name Omeprazole
Package Description 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (64861-303-01)
Product NDC 64861-303
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Omeprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080301
Marketing Category Name NDA
Labeler Name Dexcel Ltd.
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Omeprazole


General Information