| NDC Code | 68382-501-77 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (68382-501-77) / 10 CAPSULE in 1 BLISTER PACK (68382-501-30) |
|---|
| Product NDC | 68382-501 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Omeprazole And Sodium Bicarbonate |
|---|
| Non-Proprietary Name | Omeprazole And Sodium Bicarbonate |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180529 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203290 |
|---|
| Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|
| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
|---|
| Strength | 20; 1100 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
|---|