NDC 0093-5501 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-5501 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA075913 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2004-02-19 |
Marketing End Date | 2014-10-31 |