NDC 63629-7678 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-7678 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-11-23 |
Marketing End Date | 2018-06-30 |