NDC 16590-856 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-856 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA075028 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1998-07-20 | 
| Inactivation Date | 2019-10-29 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075028 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 1998-07-20 | 
| Inactivation Date | 2019-10-29 | 
| Marketing Category | ANDA | 
| Application Number | ANDA075028 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1998-07-20 | 
| Inactivation Date | 2019-10-29 |