NDC 54505-102 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 54505-102 |
Marketing Category | / |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020800 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-01 |
Marketing End Date | 2018-05-31 |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020800 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-01 |
Marketing End Date | 2018-05-31 |