NDC 0113-0271 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0113-0271 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076760 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-05-21 |
Marketing End Date | 2015-01-02 |
Marketing Category | ANDA |
Application Number | ANDA076760 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2009-05-21 |
Marketing End Date | 2015-01-02 |