NDC 99207-461

NDC 99207-461

NDC 99207-461 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 99207-461
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 99207-461-90 [99207046190]

Solodyn TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA050808
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-05-08
Marketing End Date2009-07-28

NDC 99207-461-10 [99207046110]

Solodyn TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA050808
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-05-08
Marketing End Date2013-05-31

NDC 99207-461-30 [99207046130]

Solodyn TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA050808
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-05-08
Marketing End Date2013-05-31

NDC 99207-461-01 [99207046101]

Solodyn TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA050808
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-05-08
Marketing End Date2013-05-31

Drug Details


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