NDC 68453-850 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68453-850 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020353 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1996-01-05 |
Marketing End Date | 2013-10-31 |