NDC 0093-7327 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0093-7327 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA077489 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2007-02-07 |
Marketing End Date | 2016-08-31 |