NDC 0009-5135

NDC 0009-5135

NDC 0009-5135 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0009-5135
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0009-5135-02 [00009513502]

Zyvox TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021130
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-04-18
Marketing End Date2018-07-31

NDC 0009-5135-03 [00009513503]

Zyvox TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021130
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2000-04-18
Marketing End Date2018-02-28

NDC 0009-5135-01 [00009513501]

Zyvox TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021130
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2000-04-18
Marketing End Date2018-07-31

Drug Details

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