NDC 0172-2931 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-2931 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA070098 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-02-20 |
| Marketing End Date | 2010-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA070098 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-02-20 |
| Marketing End Date | 2010-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA070098 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1986-02-20 |
| Marketing End Date | 2010-09-30 |
| Marketing Category | ANDA |
| Application Number | ANDA070098 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2012-06-08 |
| Marketing End Date | 2010-09-30 |