NDC 42549-621

NDC 42549-621

NDC 42549-621 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 42549-621
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 42549-621-90 [42549062190]

TOPIRAMATE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090278
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-03-27
Inactivation Date2019-11-13

NDC 42549-621-30 [42549062130]

TOPIRAMATE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090278
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-03-27
Inactivation Date2019-11-13

NDC 42549-621-60 [42549062160]

TOPIRAMATE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090278
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-03-27
Inactivation Date2019-11-13

NDC 42549-621-12 [42549062112]

TOPIRAMATE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA090278
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-03-27
Inactivation Date2019-11-13

Drug Details

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