NDC 0006-0711 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0006-0711 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020830 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-02-20 |
Marketing End Date | 2015-01-31 |
Marketing Category | NDA |
Application Number | NDA020830 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-02-20 |
Marketing End Date | 2013-09-19 |
Marketing Category | NDA |
Application Number | NDA020830 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-02-20 |
Marketing End Date | 2015-01-31 |
Marketing Category | NDA |
Application Number | NDA020830 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-01-15 |
Marketing End Date | 2014-06-10 |
Marketing Category | NDA |
Application Number | NDA020830 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-02-20 |
Marketing End Date | 2013-09-19 |