NDC 0186-5042 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0186-5042 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021153 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2001-03-19 |
Marketing End Date | 2015-11-06 |
Marketing Category | NDA |
Application Number | NDA021153 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2001-03-19 |
Marketing End Date | 2015-11-06 |