NDC 49999-847 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 49999-847 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-13 |
Marketing End Date | 2014-06-01 |
Marketing Category | ANDA |
Application Number | ANDA076438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-13 |
Marketing End Date | 2014-06-01 |
Marketing Category | ANDA |
Application Number | ANDA076438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-08-19 |
Marketing End Date | 2018-12-14 |
Marketing Category | ANDA |
Application Number | ANDA076438 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-12-13 |
Marketing End Date | 2014-06-01 |