NDC 0603-3740 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-3740 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076796 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2004-03-26 |
| Marketing End Date | 2016-04-21 |
| Marketing Category | ANDA |
| Application Number | ANDA076796 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-03-26 |
| Marketing End Date | 2018-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076796 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-03-26 |
| Marketing End Date | 2018-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076796 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-03-26 |
| Marketing End Date | 2018-09-30 |