NDC 71335-0837 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 71335-0837 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077890 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-30 |
Marketing End Date | 2018-06-01 |
Marketing Category | ANDA |
Application Number | ANDA077890 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-30 |
Marketing End Date | 2018-06-01 |
Marketing Category | ANDA |
Application Number | ANDA077890 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-05-30 |
Marketing End Date | 2018-06-01 |