| NDC Code: |
52125-765 |
| Proprietary Name: |
Glipizide and Metformin Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
Glipizide and Metformin Hydrochloride |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
12-11-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA077270 |
| Labeler: |
REMEDYREPACK INC. |
| Substance Name: |
GLIPIZIDE; METFORMIN HYDROCHLORIDE |
| Active Numerator Strength: |
2.5; 250 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
| DEA Schedule: |
|
