NDC 0093-4232 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-4232 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074225 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2007-10-16 |
| Marketing End Date | 2018-03-31 |