NDC 42549-606 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42549-606 | 
| Marketing Category | / | 
| Marketing Category | NDA | 
| Application Number | NDA021234 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2008-06-08 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | NDA | 
| Application Number | NDA021234 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2008-06-08 |