NDC 0093-2061

NDC 0093-2061

NDC 0093-2061 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0093-2061
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0093-2061-98 [00093206198]

Fenofibrate TABLET
Marketing CategoryNDA authorized generic
Application NumberNDA021656
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2004-11-05
Marketing End Date2018-12-31

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.