NDC 67425-999 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 67425-999 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA021664 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2010-09-20 |
Marketing End Date | 2017-12-29 |
Marketing Category | NDA |
Application Number | NDA021664 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2010-09-20 |
Marketing End Date | 2017-12-29 |
Marketing Category | NDA |
Application Number | NDA021664 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2010-09-20 |
Marketing End Date | 2017-12-29 |