| NDC Code | 54868-5210-1 |
|---|
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5210-1) |
|---|
| Product NDC | 54868-5210 |
|---|
| 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 | 20050118 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076467 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | GLIPIZIDE |
|---|
| Strength | 5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient] |
|---|