NDC 0173-0750

NDC 0173-0750

NDC 0173-0750 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0173-0750
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0173-0750-62 [00173075062]

TREXIMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021926
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2008-04-25
Marketing End Date2016-10-31

NDC 0173-0750-49 [00173075049]

TREXIMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021926
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-04-25
Marketing End Date2018-07-31

NDC 0173-0750-00 [00173075000]

TREXIMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021926
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-04-25
Marketing End Date2015-12-25

NDC 0173-0750-03 [00173075003]

TREXIMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021926
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-06-15
Marketing End Date2012-11-12

NDC 0173-0750-61 [00173075061]

TREXIMET TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA021926
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2011-10-18
Marketing End Date2014-04-08

Drug Details

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