NDC 63739-113 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63739-113 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA018569 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-10-01 |
Marketing End Date | 2012-10-31 |