NDC 16729-029 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 16729-029 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA070070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2012-06-27 |
Marketing End Date | 2012-06-27 |