NDC 0143-1265 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0143-1265 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA076063 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2015-02-24 |
| Marketing Category | ANDA |
| Application Number | ANDA076063 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2015-02-24 |
| Marketing Category | ANDA |
| Application Number | ANDA076063 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2015-02-24 |
| Marketing Category | ANDA |
| Application Number | ANDA076063 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2002-07-01 |
| Marketing End Date | 2014-10-21 |