NDC 0172-5313 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-5313 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076089 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-10-19 |
| Marketing End Date | 2013-12-05 |
| Marketing Category | ANDA |
| Application Number | ANDA076089 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-06-09 |
| Marketing End Date | 2013-12-05 |
| Marketing Category | ANDA |
| Application Number | ANDA076089 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2004-06-09 |
| Marketing End Date | 2018-11-30 |