Omeprazole - 21695-097-60 - (omeprazole)

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Drug Information of Omeprazole

Product NDC: 21695-097
Proprietary Name: Omeprazole
Non Proprietary Name: omeprazole
Active Ingredient(s): 10    mg/1 & nbsp;   omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole

Product NDC: 21695-097
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075410
Marketing Category: ANDA
Start Marketing Date: 20030903

Package Information of Omeprazole

Package NDC: 21695-097-60
Package Description: 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (21695-097-60)

NDC Information of Omeprazole

NDC Code 21695-097-60
Proprietary Name Omeprazole
Package Description 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (21695-097-60)
Product NDC 21695-097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20030903
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name OMEPRAZOLE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole


General Information