NDC 0781-2228 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0781-2228 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA071529 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1987-06-24 |
| Marketing End Date | 2016-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA071529 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1987-06-24 |
| Marketing End Date | 2016-01-31 |
| Marketing Category | ANDA |
| Application Number | ANDA071529 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1987-06-24 |
| Marketing End Date | 2016-01-31 |