Zegerid - 54868-5611-0 - (omeprazole, sodium bicarbonate)

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Drug Information of Zegerid

Product NDC: 54868-5611
Proprietary Name: Zegerid
Non Proprietary Name: omeprazole, sodium bicarbonate
Active Ingredient(s): 40; 1100    mg/1; mg/1 & nbsp;   omeprazole, sodium bicarbonate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zegerid

Product NDC: 54868-5611
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021849
Marketing Category: NDA
Start Marketing Date: 20060608

Package Information of Zegerid

Package NDC: 54868-5611-0
Package Description: 30 CAPSULE in 1 BOTTLE (54868-5611-0)

NDC Information of Zegerid

NDC Code 54868-5611-0
Proprietary Name Zegerid
Package Description 30 CAPSULE in 1 BOTTLE (54868-5611-0)
Product NDC 54868-5611
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name omeprazole, sodium bicarbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060608
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name OMEPRAZOLE; SODIUM BICARBONATE
Strength Number 40; 1100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Zegerid


General Information