| NDC Code | 33261-835-30 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (33261-835-30) |
|---|
| Product NDC | 33261-835 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glipizideer |
|---|
| Proprietary Name Suffix | Er |
|---|
| Non-Proprietary Name | Glipizide |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20031107 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076467 |
|---|
| Manufacturer | Aidarex Pharmaceuticals LLC |
|---|
| Substance Name | GLIPIZIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [CS] |
|---|