NDC 70655-077 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 70655-077 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA210989 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-31 |
Marketing End Date | 2019-12-31 |
Marketing Category | ANDA |
Application Number | ANDA210989 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-31 |
Marketing End Date | 2019-12-31 |
Marketing Category | ANDA |
Application Number | ANDA210989 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-12-31 |
Marketing End Date | 2019-12-31 |