NDC 50484-322 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 50484-322 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part347 |
Product Type | HUMAN OTC DRUG |
Billing Unit | GM |
Marketing Start Date | 2005-08-01 |
Marketing End Date | 2018-07-31 |
Marketing Category | OTC monograph final |
Application Number | part347 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2005-08-01 |
Marketing End Date | 2018-07-31 |