NDC 68220-142 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 68220-142 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA086195 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1978-07-26 |
| Marketing End Date | 2018-07-31 |