NDC 0591-3774 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0591-3774 |
Marketing Category | / |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020702 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-12-17 |
Marketing End Date | 2015-10-31 |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020702 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-17 |
Marketing End Date | 2015-10-31 |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020702 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-12-17 |
Marketing End Date | 2015-10-31 |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA020702 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1996-12-17 |
Marketing End Date | 2015-10-31 |