NDC 0182-1061 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0182-1061 |
Marketing Category | / |
Marketing Category | OTC monograph final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 1994-02-05 |
Marketing End Date | 2013-05-30 |