NDC 0074-6123 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0074-6123 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021656 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2004-11-05 |
Marketing End Date | 2015-07-14 |
Marketing Category | NDA |
Application Number | NDA021656 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-11-05 |
Marketing End Date | 2019-01-24 |