NDC 0093-1016

NDC 0093-1016

NDC 0093-1016 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0093-1016
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0093-1016-98 [00093101698]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075189
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-06-15
Marketing End Date2013-08-06

NDC 0093-1016-01 [00093101601]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075189
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2001-09-26
Marketing End Date2018-04-30

NDC 0093-1016-93 [00093101693]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075189
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-12-21
Marketing End Date2013-08-31

NDC 0093-1016-19 [00093101619]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075189
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-20
Marketing End Date2018-04-30

NDC 0093-1016-10 [00093101610]

Nabumetone TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075189
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-02-24
Marketing End Date2017-12-31

Drug Details

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