NDC 0093-5711 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-5711 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-05-02 |
| Marketing End Date | 2013-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-05-07 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-10-08 |
| Marketing End Date | 2016-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-05-07 |
| Marketing End Date | 2016-12-31 |