NDC 42291-691 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42291-691 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA200900 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-09-29 |
Marketing End Date | 2018-11-19 |