NDC 16714-582 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16714-582 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA090382 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-10-03 | 
| Marketing End Date | 2015-03-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA090382 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-10-03 | 
| Marketing End Date | 2015-03-31 | 
| Marketing Category | ANDA | 
| Application Number | ANDA090382 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2010-10-03 | 
| Marketing End Date | 2015-03-31 |