NDC 68382-077 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 68382-077 |
Marketing Category | / |
Marketing Category | NDA authorized generic |
Application Number | NDA022224 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2008-12-15 |
Marketing End Date | 2019-03-23 |