NDC 49884-685 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 49884-685 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070581 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1985-10-17 |
| Marketing End Date | 2019-01-23 |
| Marketing Category | ANDA |
| Application Number | ANDA070581 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1985-10-17 |
| Marketing End Date | 2019-01-23 |