NDC 0172-3626 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-3626 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA062505 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2011-02-10 |
| Marketing End Date | 2013-09-05 |
| Marketing Category | ANDA |
| Application Number | ANDA062505 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1984-09-11 |
| Marketing End Date | 2014-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA062505 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1984-09-11 |
| Marketing End Date | 2014-07-31 |
| Marketing Category | ANDA |
| Application Number | ANDA062505 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2011-02-10 |
| Marketing End Date | 2013-09-05 |