NDC 60505-0192 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 60505-0192 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090666 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-07 |
Marketing End Date | 2013-12-13 |
Marketing Category | ANDA |
Application Number | ANDA090666 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-12-07 |
Marketing End Date | 2016-10-01 |
Marketing Category | ANDA |
Application Number | ANDA090666 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-07 |
Marketing End Date | 2016-10-01 |
Marketing Category | ANDA |
Application Number | ANDA090666 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-07 |
Marketing End Date | 2016-10-01 |
Marketing Category | ANDA |
Application Number | ANDA090666 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-07 |
Marketing End Date | 2016-10-01 |
Marketing Category | ANDA |
Application Number | ANDA090666 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2011-12-07 |
Marketing End Date | 2016-10-01 |