NDC 46122-205 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 46122-205 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075400 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2009-10-07 |
Marketing End Date | 2019-01-22 |
Marketing Category | ANDA |
Application Number | ANDA075400 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-10-07 |
Marketing End Date | 2019-01-22 |