NDC 67253-142 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 67253-142 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062927 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 1988-11-25 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA062927 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1988-11-25 |
| Marketing End Date | 2015-12-31 |
| Marketing Category | ANDA |
| Application Number | ANDA062927 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1988-11-25 |
| Marketing End Date | 2015-12-31 |