| NDC Code: |
59762-2331 |
| Proprietary Name: |
Glyburide and Metformin Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
Glyburide and Metformin Hydrochloride |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
14-11-2007 |
| Category Name: |
ANDA |
| Application Number: |
ANDA077870 |
| Labeler: |
GREENSTONE LLC |
| Substance Name: |
GLYBURIDE; METFORMIN HYDROCHLORIDE |
| Active Numerator Strength: |
2.5; 500 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient],Biguanide [EPC],Biguanides [Chemical/Ingredient] |
| DEA Schedule: |
|
