NDC 59011-334

NDC 59011-334

NDC 59011-334 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 59011-334
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 59011-334-60 [59011033460]

RYZOLT TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021745
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-02-16
Marketing End Date2013-09-30

NDC 59011-334-30 [59011033430]

RYZOLT TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021745
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-12-15
Marketing End Date2013-09-30

NDC 59011-334-90 [59011033490]

RYZOLT TABLET, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA021745
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-12-15
Marketing End Date2013-09-30

Drug Details

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