NDC 64011-010 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 64011-010 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA018238 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-08-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | NDA |
Application Number | NDA018238 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-08-01 |
Inactivation Date | 2019-10-21 |
Marketing Category | NDA |
Application Number | NDA018238 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-08-01 |
Inactivation Date | 2019-10-21 |