| NDC Code | 68462-521-90 |
|---|
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-90) |
|---|
| Product NDC | 68462-521 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Metformin Hydrochloride |
|---|
| Non-Proprietary Name | Metformin Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20191125 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA212969 |
|---|
| Manufacturer | GLENMARK PHARMACEUTICALS INC., USA |
|---|
| Substance Name | METFORMIN HYDROCHLORIDE |
|---|
| Strength | 1000 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Biguanide [EPC], Biguanides [CS] |
|---|