NDC 63323-734 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 63323-734 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA076207 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2002-05-19 |
Marketing End Date | 2015-08-27 |