NDC 42291-836 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 42291-836 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA071196 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-02-06 |
Marketing End Date | 2017-09-01 |