NDC 48102-101 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 48102-101 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA040062 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2010-06-22 |
Marketing End Date | 2013-06-14 |