NDC 16590-225 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 16590-225 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA050555 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 1981-11-25 |
| Inactivation Date | 2019-10-29 |
| Marketing Category | NDA |
| Application Number | NDA021745 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2011-02-07 |
| Marketing Category | NDA |
| Application Number | NDA021745 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2011-02-07 |
| Marketing Category | NDA |
| Application Number | NDA021745 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-12-30 |
| Marketing End Date | 2011-02-07 |