NDC 0004-6202 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0004-6202 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA018164 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1980-09-04 |
Marketing End Date | 2017-01-31 |