NDC 0264-9011 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0264-9011 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA016822 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1971-09-24 |
Marketing End Date | 2012-05-01 |