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