NDC 16590-082 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-082 | 
| Marketing Category | / | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-09-11 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 1984-05-07 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-09-11 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-09-11 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Marketing Start Date | 1984-05-07 | 
| Marketing End Date | 2012-09-11 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2012-09-11 | 
| Inactivation Date | 2019-11-13 | 
| Marketing Category | ANDA | 
| Application Number | ANDA062396 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 1984-05-07 | 
| Inactivation Date | 2019-11-13 |