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omeprazole/sodium bicarbonate - 66993-413-30 - (omeprazole, sodium bicarbonate)

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Drug Information of omeprazole/sodium bicarbonate

Product NDC: 66993-413
Proprietary Name: omeprazole/sodium bicarbonate
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 omeprazole/sodium bicarbonate

Product NDC: 66993-413
Labeler Name: Prasco, Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021849
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20060227

Package Information of omeprazole/sodium bicarbonate

Package NDC: 66993-413-30
Package Description: 30 CAPSULE in 1 BOTTLE (66993-413-30)

NDC Information of omeprazole/sodium bicarbonate

NDC Code 66993-413-30
Proprietary Name omeprazole/sodium bicarbonate
Package Description 30 CAPSULE in 1 BOTTLE (66993-413-30)
Product NDC 66993-413
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name omeprazole, sodium bicarbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20060227
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Prasco, Laboratories
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 omeprazole/sodium bicarbonate


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