NDC 0093-5118 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0093-5118 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA075116 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1999-12-28 |
| Marketing End Date | 2018-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA075116 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1999-12-28 |
| Marketing End Date | 1999-12-28 |