| NDC Code | 68071-4020-9 |
|---|
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4020-9) |
|---|
| Product NDC | 68071-4020 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glipizide |
|---|
| Non-Proprietary Name | Glipizide |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20161221 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076159 |
|---|
| Manufacturer | NuCare Pharmaceuticals,Inc. |
|---|
| Substance Name | GLIPIZIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [CS] |
|---|