| NDC Code | 60429-725-05 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60429-725-05) |
|---|
| Product NDC | 60429-725 |
|---|
| 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 | 20060829 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076172 |
|---|
| Manufacturer | Golden State Medical Supply, Inc. |
|---|
| Substance Name | METFORMIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Biguanide [EPC],Biguanides [Chemical/Ingredient] |
|---|