NDC 0173-0570 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0173-0570 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020781 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1999-03-01 |
Marketing End Date | 2011-09-22 |
Marketing Category | NDA |
Application Number | NDA020781 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1999-03-01 |
Marketing End Date | 2018-02-28 |