NDC 0185-0139 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0185-0139 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074903 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-04-19 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074903 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1999-04-19 |
| Marketing End Date | 2017-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074903 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-04-19 |
| Marketing End Date | 2017-12-31 |