| NDC Code | 21695-894-00 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (21695-894-00) |
|---|
| Product NDC | 21695-894 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Glipizide And Metformin Hydrochloride |
|---|
| Non-Proprietary Name | Glipizide And Metformin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100312 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077270 |
|---|
| Manufacturer | Rebel Distributors Corp |
|---|
| Substance Name | GLIPIZIDE; METFORMIN HYDROCHLORIDE |
|---|
| Strength | 5; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Sulfonylurea [EPC],Sulfonylurea Compounds [CS],Biguanide [EPC],Biguanides [CS] |
|---|