Omeprazole - 21695-617-90 - (Omeprazole)

Alphabetical Index


Drug Information of Omeprazole

Product NDC: 21695-617
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 40    mg/1 & nbsp;   Omeprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole

Product NDC: 21695-617
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075576
Marketing Category: ANDA
Start Marketing Date: 20101013

Package Information of Omeprazole

Package NDC: 21695-617-90
Package Description: 90 CAPSULE in 1 BOTTLE (21695-617-90)

NDC Information of Omeprazole

NDC Code 21695-617-90
Proprietary Name Omeprazole
Package Description 90 CAPSULE in 1 BOTTLE (21695-617-90)
Product NDC 21695-617
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101013
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name OMEPRAZOLE
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole


General Information