NDC 47682-808 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 47682-808 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075139 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-30 |
Marketing End Date | 2018-02-01 |
Marketing Category | ANDA |
Application Number | ANDA075139 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-30 |
Marketing End Date | 2018-02-01 |
Marketing Category | ANDA |
Application Number | ANDA075139 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-30 |
Marketing End Date | 2018-02-01 |
Marketing Category | ANDA |
Application Number | ANDA075139 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-30 |
Marketing End Date | 2018-02-01 |
Marketing Category | ANDA |
Application Number | ANDA075139 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-30 |
Marketing End Date | 2018-02-01 |