| NDC Code | 51991-642-01 |
|---|
| Package Description | 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-642-01) |
|---|
| Product NDC | 51991-642 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Omeprazole |
|---|
| Non-Proprietary Name | Omeprazole |
|---|
| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170703 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203481 |
|---|
| Manufacturer | Breckenridge Pharmaceutical, Inc. |
|---|
| Substance Name | OMEPRAZOLE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA] |
|---|