NDC 0603-5781 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-5781 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA078060 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2007-01-25 | 
| Marketing End Date | 2018-01-17 | 
| Marketing Category | ANDA | 
| Application Number | ANDA078060 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2007-01-25 | 
| Marketing End Date | 2018-01-17 | 
| Marketing Category | ANDA | 
| Application Number | ANDA078060 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2007-01-25 | 
| Marketing End Date | 2018-01-17 |