NDC 0781-1717 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-1717 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA080439 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1973-01-03 |
| Marketing End Date | 2014-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA080439 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1973-01-03 |
| Marketing End Date | 2014-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA080439 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1973-01-03 |
| Marketing End Date | 2014-03-31 |