NDC 0172-4285 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0172-4285 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA073568 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-10-10 |
| Marketing End Date | 2014-03-07 |
| Marketing Category | ANDA |
| Application Number | ANDA073568 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1997-10-10 |
| Marketing End Date | 2015-03-31 |
| Marketing Category | ANDA |
| Application Number | ANDA073568 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2009-09-03 |
| Marketing End Date | 2014-03-07 |
| Marketing Category | ANDA |
| Application Number | ANDA073568 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1997-10-10 |
| Marketing End Date | 2009-09-03 |