NDC 42549-522 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42549-522 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040189 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-10-31 |
| Inactivation Date | 2019-11-13 |