NDC 45963-141 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 45963-141 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA077285 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2016-02-12 |
| Marketing End Date | 2016-09-26 |
| Marketing Category | ANDA |
| Application Number | ANDA077285 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-02-05 |
| Marketing End Date | 2017-10-31 |
| Marketing Category | ANDA |
| Application Number | ANDA077285 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2015-02-05 |
| Marketing End Date | 2016-09-26 |