NDC 0093-7438 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-7438 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077470 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-06-24 |
| Marketing End Date | 2008-06-24 |
| Marketing Category | ANDA |
| Application Number | ANDA077470 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-06-24 |
| Marketing End Date | 2010-04-06 |
| Marketing Category | ANDA |
| Application Number | ANDA077470 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2008-06-24 |
| Marketing End Date | 2016-03-31 |