NDC 67253-741 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67253-741 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074270 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1993-09-27 |
| Marketing End Date | 2015-02-23 |
| Marketing Category | ANDA |
| Application Number | ANDA074270 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-09-27 |
| Marketing End Date | 2018-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA074270 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-09-27 |
| Marketing End Date | 2018-03-31 |