| NDC Code | 70954-798-20 |
|---|
| Package Description | 30 PACKET in 1 CARTON (70954-798-20) / 1 POWDER, FOR SUSPENSION in 1 PACKET (70954-798-10) |
|---|
| Product NDC | 70954-798 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Omeprazole And Sodium Bicarbonate |
|---|
| Non-Proprietary Name | Omeprazole And Sodium Bicarbonate |
|---|
| Dosage Form | POWDER, FOR SUSPENSION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20260115 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA219161 |
|---|
| Manufacturer | ANI Pharmaceuticals, Inc. |
|---|
| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
|---|
| Strength | 40; 1680 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
|---|