Home > National Drug Code (NDC) > Omeprazole and Sodium Bicarbonate

Omeprazole and Sodium Bicarbonate - 49884-397-05 - (Omeprazole and Sodium Bicarbonate)

Alphabetical Index


Drug Information of Omeprazole and Sodium Bicarbonate

Product NDC: 49884-397
Proprietary Name: Omeprazole and Sodium Bicarbonate
Non Proprietary Name: Omeprazole and Sodium Bicarbonate
Active Ingredient(s): 20; 1100    mg/1; mg/1 & nbsp;   Omeprazole and Sodium Bicarbonate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Omeprazole and Sodium Bicarbonate

Product NDC: 49884-397
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078966
Marketing Category: ANDA
Start Marketing Date: 20100701

Package Information of Omeprazole and Sodium Bicarbonate

Package NDC: 49884-397-05
Package Description: 500 CAPSULE in 1 BOTTLE (49884-397-05)

NDC Information of Omeprazole and Sodium Bicarbonate

NDC Code 49884-397-05
Proprietary Name Omeprazole and Sodium Bicarbonate
Package Description 500 CAPSULE in 1 BOTTLE (49884-397-05)
Product NDC 49884-397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omeprazole and Sodium Bicarbonate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100701
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc.
Substance Name OMEPRAZOLE; SODIUM BICARBONATE
Strength Number 20; 1100
Strength Unit mg/1; mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Omeprazole and Sodium Bicarbonate


General Information