NDC Code | 60760-568-90 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-568-90) |
Product NDC | 60760-568 |
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 | 20180918 |
Marketing Category Name | ANDA |
Application Number | ANDA204720 |
Manufacturer | St. Mary's Medical Park Pharmacy |
Substance Name | GLIPIZIDE |
Strength | 10 |
Strength Unit | mg/1 |
Pharmacy Classes | Sulfonylurea Compounds [CS], Sulfonylurea [EPC] |