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Zegerid
Zegerid - 68012-052-30 - (omeprazole, sodium bicarbonate)
Drug Information of Zegerid
| Product NDC: | 68012-052 |
| Proprietary Name: | Zegerid |
| Non Proprietary Name: | omeprazole, sodium bicarbonate |
| Active Ingredient(s): | 20; 1680 mg/1; mg/1 & nbsp; omeprazole, sodium bicarbonate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Zegerid
| Product NDC: | 68012-052 |
| Labeler Name: | Santarus, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021636 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20040615 |
Package Information of Zegerid
| Package NDC: | 68012-052-30 |
| Package Description: | 30 PACKET in 1 CARTON (68012-052-30) > 1 POWDER, FOR SUSPENSION in 1 PACKET (68012-052-01) |
NDC Information of Zegerid
| NDC Code | 68012-052-30 |
| Proprietary Name | Zegerid |
| Package Description | 30 PACKET in 1 CARTON (68012-052-30) > 1 POWDER, FOR SUSPENSION in 1 PACKET (68012-052-01) |
| Product NDC | 68012-052 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | omeprazole, sodium bicarbonate |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20040615 |
| Marketing Category Name | NDA |
| Labeler Name | Santarus, Inc. |
| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
| Strength Number | 20; 1680 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
