NDC 50111-852 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50111-852 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073484 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-10-31 |
| Marketing End Date | 2017-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA073484 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1993-10-31 |
| Marketing End Date | 2012-11-28 |