Omeprazole - 68788-9955-1 - (Omeprazole)

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Drug Information of Omeprazole

Product NDC: 68788-9955
Proprietary Name: Omeprazole
Non Proprietary Name: Omeprazole
Active Ingredient(s): 20    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: 68788-9955
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076048
Marketing Category: ANDA
Start Marketing Date: 20120110

Package Information of Omeprazole

Package NDC: 68788-9955-1
Package Description: 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9955-1)

NDC Information of Omeprazole

NDC Code 68788-9955-1
Proprietary Name Omeprazole
Package Description 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-9955-1)
Product NDC 68788-9955
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120110
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name OMEPRAZOLE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole


General Information