NDC 53746-119 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 53746-119 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA040813 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2007-02-23 | 
| Marketing End Date | 2014-04-01 | 
| Marketing Category | ANDA | 
| Application Number | ANDA040813 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2007-02-23 | 
| Marketing End Date | 2014-04-01 | 
| Marketing Category | ANDA | 
| Application Number | ANDA040813 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2007-02-23 | 
| Marketing End Date | 2014-04-01 |