NDC 76282-322 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 76282-322 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-26 |
Marketing End Date | 2018-09-12 |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-04-26 |
Marketing End Date | 2018-09-12 |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-20 |
Marketing End Date | 2018-09-12 |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-20 |
Marketing End Date | 2018-09-12 |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-20 |
Marketing End Date | 2018-09-12 |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-20 |
Marketing End Date | 2018-09-12 |
Marketing Category | ANDA |
Application Number | ANDA090705 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-03-20 |
Marketing End Date | 2018-09-12 |