| NDC Code | 51407-814-05 |
|---|
| Package Description | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-814-05) |
|---|
| Product NDC | 51407-814 |
|---|
| 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 | Golden State Medical Supply, Inc. |
|---|
| Substance Name | OMEPRAZOLE |
|---|
| Strength | 40 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
|---|