NDC 0173-0446 is a in the category. It is labeled and distributed by .
| Proprietary Name | NDC 0173-0446 |
| Marketing Category | / |
| Marketing Category | NDA |
| Application Number | NDA020103 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-02-11 |
| Marketing End Date | 2019-02-28 |
| Marketing Category | NDA |
| Application Number | NDA020103 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 1993-02-11 |
| Marketing End Date | 2011-09-22 |
| Marketing Category | NDA |
| Application Number | NDA020103 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 1993-02-11 |
| Marketing End Date | 2013-12-16 |