NDC 50742-101 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50742-101 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077877 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-01-30 |
| Marketing End Date | 2017-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077877 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-01-30 |
| Marketing End Date | 2017-05-31 |