NDC 62037-675 is a Tablet, Film Coated in the Bulk Ingredient category. It is labeled and distributed by Actavis Pharma, Inc..
| Product ID | 62037-675_f732d7c8-a2c9-4137-ba89-eb278b158df8 |
| NDC | 62037-675 |
| Product Type | Bulk Ingredient |
| Proprietary Name | NDC 62037-675 |
| Dosage Form | Tablet, Film Coated |
| Marketing Start Date | 2002-01-25 |
| Marketing Category | / DRUG FOR FURTHER PROCESSING |
| Labeler Name | Actavis Pharma, Inc. |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075961 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-25 |
| Marketing End Date | 2016-06-21 |
| Marketing Category | ANDA |
| Application Number | ANDA075961 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-25 |
| Marketing End Date | 2016-06-21 |
| Marketing Category | ANDA |
| Application Number | ANDA075961 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-01-25 |
| Marketing End Date | 2016-06-21 |
| Ingredient | Strength |
|---|---|
| METFORMIN HYDROCHLORIDE | 850 mg/1 |