Omeprazole - 55111-159-01 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 55111-159
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 40    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: 55111-159
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075576
Marketing Category: ANDA
Start Marketing Date: 20090121

Package Information of Omeprazole

Package NDC: 55111-159-01
Package Description: 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-159-01)

NDC Information of Omeprazole

NDC Code 55111-159-01
Proprietary Name Omeprazole
Package Description 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-159-01)
Product NDC 55111-159
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20090121
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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