NDC 0093-3195 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-3195 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-01-01 |
| Marketing End Date | 2019-02-28 |
| Marketing Category | ANDA |
| Application Number | ANDA073517 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-01-01 |
| Marketing End Date | 2019-02-28 |