NDC Code | 54868-5210-2 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5210-2) |
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] |