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omeprazole/sodium bicarbonate
omeprazole/sodium bicarbonate - 66993-412-30 - (omeprazole, sodium bicarbonate)
Drug Information of omeprazole/sodium bicarbonate
| Product NDC: | 66993-412 |
| Proprietary Name: | omeprazole/sodium bicarbonate |
| Non Proprietary Name: | omeprazole, sodium bicarbonate |
| Active Ingredient(s): | 20; 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: | 66993-412 |
| 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: | 66993-412-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (66993-412-30) |
NDC Information of omeprazole/sodium bicarbonate
| NDC Code | 66993-412-30 |
| Proprietary Name | omeprazole/sodium bicarbonate |
| Package Description | 30 CAPSULE in 1 BOTTLE (66993-412-30) |
| Product NDC | 66993-412 |
| 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 | 20; 1100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
