NDC 99207-462 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 99207-462 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA050808 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-05-08 |
Marketing End Date | 2014-02-28 |
Marketing Category | NDA |
Application Number | NDA050808 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-05-08 |
Marketing End Date | 2014-02-28 |
Marketing Category | NDA |
Application Number | NDA050808 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2006-05-08 |
Marketing End Date | 2014-02-28 |
Marketing Category | NDA |
Application Number | NDA050808 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2006-05-08 |
Marketing End Date | 2009-07-28 |