| NDC Code | 68788-9269-1 |
|---|
| Package Description | 14 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68788-9269-1) |
|---|
| Product NDC | 68788-9269 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lansoprazole |
|---|
| Non-Proprietary Name | Lansoprazole |
|---|
| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090763 |
|---|
| Manufacturer | Preferred Pharmaceuticals, Inc. |
|---|
| Substance Name | LANSOPRAZOLE |
|---|
| Strength | 30 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE] |
|---|