NDC 70655-015 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 70655-015 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA210231 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-08-29 |
Marketing End Date | 2019-06-28 |
Marketing Category | ANDA |
Application Number | ANDA210231 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-06-28 |
Marketing End Date | 2019-06-28 |