NDC 51079-881 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 51079-881 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075150 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1997-07-15 |
Marketing End Date | 2017-04-30 |
Marketing Category | ANDA |
Application Number | ANDA075150 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-03-15 |
Marketing End Date | 2017-04-30 |
Marketing Category | ANDA |
Application Number | ANDA075150 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-07-15 |
Marketing End Date | 2017-04-30 |
Marketing Category | ANDA |
Application Number | ANDA075150 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-08-01 |
Marketing End Date | 2016-07-31 |
Marketing Category | ANDA |
Application Number | ANDA075150 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1997-07-15 |
Marketing End Date | 2017-04-30 |