NDC 0093-5710 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-5710 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-06-19 |
| Marketing End Date | 2010-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-03-04 |
| Marketing End Date | 2016-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-06-14 |
| Marketing End Date | 2016-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-06-14 |
| Marketing End Date | 2016-11-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076345 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2007-09-28 |
| Marketing End Date | 2008-10-31 |