NDC 63629-6659 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-6659 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA087342 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-10 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA087342 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-10 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA087342 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-10 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA087342 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-10 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA087342 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-10 |
Marketing End Date | 2018-08-31 |
Marketing Category | ANDA |
Application Number | ANDA087342 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2015-08-10 |
Marketing End Date | 2018-08-31 |