NDC 0093-0739 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-0739 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA090425 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-05-31 |
| Marketing End Date | 2015-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA090425 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-05-31 |
| Marketing End Date | 2015-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA090425 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-05-31 |
| Marketing End Date | 2015-07-31 |