NDC 50383-282 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 50383-282 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076673 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-01-21 |
| Marketing End Date | 2017-08-26 |
| Marketing Category | ANDA |
| Application Number | ANDA076673 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-01-21 |
| Marketing End Date | 2017-08-26 |
| Marketing Category | ANDA |
| Application Number | ANDA076673 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-01-21 |
| Marketing End Date | 2017-08-26 |