NDC 63739-111 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 63739-111 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA018569 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2004-10-01 | 
| Marketing End Date | 2012-10-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA018569 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 2004-10-01 | 
| Marketing End Date | 2012-10-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA018569 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2004-10-01 | 
| Marketing End Date | 2012-10-31 |