NDC 0172-4286 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-4286 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA074330 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2009-09-03 |
| Marketing End Date | 2015-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074330 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-08-01 |
| Marketing End Date | 2015-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074330 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-08-01 |
| Marketing End Date | 2015-04-30 |
| Marketing Category | ANDA |
| Application Number | ANDA074330 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1992-08-01 |
| Marketing End Date | 2009-09-03 |
| Marketing Category | ANDA |
| Application Number | ANDA074330 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1992-08-01 |
| Marketing End Date | 2015-04-30 |