NDC 76218-0708 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 76218-0708 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA022370 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-03-14 |
Marketing End Date | 2015-10-30 |
Marketing Category | NDA |
Application Number | NDA022370 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2012-03-14 |
Marketing End Date | 2015-10-30 |