NDC 0093-7392 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-7392 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076378 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-09-20 |
| Marketing End Date | 2018-06-30 |
| Marketing Category | ANDA |
| Application Number | ANDA076378 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2013-09-20 |
| Marketing End Date | 2018-11-30 |