NDC 0781-5020 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-5020 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA040101 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-07-19 |
| Marketing End Date | 1996-07-19 |
| Marketing Category | ANDA |
| Application Number | ANDA040101 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1996-07-19 |
| Marketing End Date | 1996-07-19 |
| Marketing Category | ANDA |
| Application Number | ANDA040101 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1996-07-19 |
| Marketing End Date | 2018-08-31 |