NDC 45802-822 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 45802-822 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077295 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2005-10-06 |
Marketing End Date | 2015-10-01 |