NDC 16590-585 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-585 |
| Marketing Category | / |
| Marketing Category | ANDA |
| Application Number | ANDA071525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1988-03-09 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA071525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1988-03-09 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA071525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1988-03-09 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA071525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1988-03-09 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | ANDA |
| Application Number | ANDA071525 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1988-03-09 |
| Inactivation Date | 2019-10-29 |