NDC 0172-2407 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-2407 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA060704 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-01-31 |
| Marketing End Date | 2014-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA060704 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-01-31 |
| Marketing End Date | 2014-05-31 |
| Marketing Category | ANDA |
| Application Number | ANDA060704 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-12 |
| Marketing End Date | 2013-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA060704 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2000-01-31 |
| Marketing End Date | 2014-04-30 |