NDC 0187-3203 is a in the category. It is labeled and distributed by .
Proprietary Name | NDC 0187-3203 |
Marketing Category | / |
Marketing Category | NDA |
Application Number | NDA016831 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1970-07-29 |
Marketing End Date | 2008-02-28 |
Marketing Category | NDA |
Application Number | NDA016831 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 1970-07-29 |
Marketing End Date | 2008-02-28 |