NDC 0603-7861 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0603-7861 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040671 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-06-09 |
| Marketing End Date | 2018-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040671 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2006-06-09 |
| Marketing End Date | 2018-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA040671 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2006-06-09 |
| Marketing End Date | 2018-12-31 |