NDC 42549-651 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42549-651 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070920 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-05-24 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA070920 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-05-24 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA070920 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-05-24 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA070920 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-05-24 |
| Inactivation Date | 2019-11-13 |