NDC 0186-1030 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0186-1030 |
Marketing Category | / |
Marketing Category | ANDA |
Application Number | ANDA070552 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2013-02-28 |
Marketing Category | ANDA |
Application Number | ANDA070552 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1990-09-30 |
Marketing End Date | 2013-10-31 |
Marketing Category | ANDA |
Application Number | ANDA070552 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1990-07-01 |
Marketing End Date | 2013-10-31 |
Marketing Category | ANDA |
Application Number | ANDA070552 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1990-07-01 |
Marketing End Date | 2014-04-30 |