NDC 49999-097 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49999-097 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2014-06-01 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2018-10-26 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2014-06-01 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2014-06-01 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2018-10-26 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2018-10-26 |
Marketing Category | ANDA |
Application Number | ANDA078558 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-11-21 |
Marketing End Date | 2014-06-01 |