NDC 0338-1071 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0338-1071 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA020255 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1993-09-27 |
Marketing End Date | 2008-12-31 |