NDC 0603-3967

NDC 0603-3967

NDC 0603-3967 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 0603-3967
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 0603-3967-28 [00603396728]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040579
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-27
Marketing End Date2016-12-31

NDC 0603-3967-10 [00603396710]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040579
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2005-05-27
Marketing End Date2016-01-28

NDC 0603-3967-21 [00603396721]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040579
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-27
Marketing End Date2016-12-31

NDC 0603-3967-32 [00603396732]

Hydroxyzine Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA040579
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2005-05-27
Marketing End Date2016-12-31

Drug Details

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