NDC 0603-3969

NDC 0603-3969

NDC 0603-3969 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0603-3969
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0603-3969-10 [00603396910]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040580
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-05-27
Marketing End Date2016-01-28

NDC 0603-3969-28 [00603396928]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040580
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-27
Marketing End Date2016-12-31

NDC 0603-3969-21 [00603396921]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040580
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-27
Marketing End Date2016-12-31

NDC 0603-3969-32 [00603396932]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040580
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-05-27
Marketing End Date2016-12-31

Drug Details

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