NDC 76439-103 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 76439-103 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA062058 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-01-12 | 
| Marketing End Date | 2015-07-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062058 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-01-12 | 
| Marketing End Date | 2015-07-13 |