NDC 63629-5007 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63629-5007 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA071745 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-05-31 |
Marketing End Date | 2018-01-30 |
Marketing Category | ANDA |
Application Number | ANDA071745 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-05-31 |
Marketing End Date | 2018-01-30 |
Marketing Category | ANDA |
Application Number | ANDA071745 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-05-31 |
Marketing End Date | 2018-01-30 |
Marketing Category | ANDA |
Application Number | ANDA071745 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-05-31 |
Marketing End Date | 2018-01-30 |
Marketing Category | ANDA |
Application Number | ANDA071745 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-05-31 |
Marketing End Date | 2018-01-30 |