NDC 0781-5754 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-5754 |
| Marketing Category | / |
| Marketing Category | NDA authorized generic |
| Application Number | NDA018029 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1982-03-31 |
| Marketing End Date | 2017-04-30 |
| Marketing Category | NDA authorized generic |
| Application Number | NDA018029 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1982-03-31 |
| Marketing End Date | 2011-07-18 |