NDC 16729-194 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16729-194 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA202554 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2014-05-16 |
Marketing End Date | 2018-01-31 |