NDC 0186-1029 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0186-1029 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA018304 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2012-01-31 |