NDC 63629-7070

NDC 63629-7070

NDC 63629-7070 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 63629-7070
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 63629-7070-3 [63629707003]

Labetalol hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075133
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-08-08
Marketing End Date2017-07-30

NDC 63629-7070-4 [63629707004]

Labetalol hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075133
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-08-08
Marketing End Date2017-07-30

NDC 63629-7070-2 [63629707002]

Labetalol hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075133
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-08-08
Marketing End Date2017-07-30

NDC 63629-7070-1 [63629707001]

Labetalol hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA075133
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-08-08
Marketing End Date2017-07-30

Drug Details

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