NDC 0074-3074

NDC 0074-3074

NDC 0074-3074 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0074-3074
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0074-3074-03 [00074307403]

Niaspan TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020381
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2015-01-05
Marketing End Date2015-04-30

NDC 0074-3074-11 [00074307411]

Niaspan TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020381
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-07-28
Marketing End Date2009-06-29

NDC 0074-3074-90 [00074307490]

Niaspan TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020381
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1997-07-28
Marketing End Date2018-11-30

NDC 0074-3074-07 [00074307407]

Niaspan TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020381
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-07-28
Marketing End Date2017-09-18

NDC 0074-3074-30 [00074307430]

Niaspan TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA020381
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1997-07-28
Marketing End Date2008-12-30

Drug Details

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.