NDC 42291-392 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 42291-392 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA076262 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2013-06-18 | 
| Marketing End Date | 2018-11-19 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076262 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2013-06-18 | 
| Marketing End Date | 2018-11-19 | 
| Marketing Category | ANDA | 
| Application Number | ANDA076262 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2013-10-28 | 
| Marketing End Date | 2015-02-24 |