NDC 0172-7171 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-7171 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074424 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1995-06-29 |
| Marketing End Date | 2012-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074424 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1995-06-29 |
| Marketing End Date | 2012-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074424 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1995-06-29 |
| Marketing End Date | 2012-04-30 |