NDC 0173-0470 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0173-0470 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020564 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1995-11-21 |
Marketing End Date | 2015-06-16 |