NDC 0603-5780 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-5780 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA078060 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-01-25 |
| Marketing End Date | 2012-06-02 |
| Marketing Category | ANDA |
| Application Number | ANDA078060 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-01-25 |
| Marketing End Date | 2012-06-02 |
| Marketing Category | ANDA |
| Application Number | ANDA078060 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-01-25 |
| Marketing End Date | 2012-06-02 |
| Marketing Category | ANDA |
| Application Number | ANDA078060 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-01-25 |
| Marketing End Date | 2012-06-02 |