| NDC Code | 51655-966-52 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-966-52) |
|---|
| Product NDC | 51655-966 |
|---|
| 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 | 20230627 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204720 |
|---|
| Manufacturer | Northwind Pharmaceuticals, LLC |
|---|
| Substance Name | GLIPIZIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |
|---|