Omeprazole - 65841-759-10 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 65841-759
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: 65841-759
Labeler Name: Cadila Healthcare Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091352
Marketing Category: ANDA
Start Marketing Date: 20121123

Package Information of Omeprazole

Package NDC: 65841-759-10
Package Description: 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-10)

NDC Information of Omeprazole

NDC Code 65841-759-10
Proprietary Name Omeprazole
Package Description 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-759-10)
Product NDC 65841-759
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20121123
Marketing Category Name ANDA
Labeler Name Cadila Healthcare Limited
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