| NDC Code | 85509-1031-1 |
|---|
| Package Description | 15 CAPSULE in 1 BOTTLE (85509-1031-1) |
|---|
| Product NDC | 85509-1031 |
|---|
| 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 | 20160715 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204228 |
|---|
| Manufacturer | PHOENIX RX LLC |
|---|
| 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] |
|---|