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 |