NDC 37205-280 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 37205-280 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075794 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-05-16 |
Marketing End Date | 2019-03-26 |
Marketing Category | ANDA |
Application Number | ANDA075794 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2002-05-16 |
Marketing End Date | 2019-03-26 |