NDC 13668-590

Cetirizine Hydrochloride

Cetirizine Hydrochloride

Cetirizine Hydrochloride is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Torrent Pharmaceuticals Limited. The primary component is Cetirizine Hydrochloride.

Product ID13668-590_30ddd5e6-1219-4f60-9b2e-3849e8a72daf
NDC13668-590
Product TypeHuman Otc Drug
Proprietary NameCetirizine Hydrochloride
Generic NameCetirizine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2010-04-15
Marketing CategoryANDA / ANDA
Application NumberANDA079191
Labeler NameTorrent Pharmaceuticals Limited
Substance NameCETIRIZINE HYDROCHLORIDE
Active Ingredient Strength5 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 13668-590-05

500 TABLET in 1 BOTTLE (13668-590-05)
Marketing Start Date2010-04-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 13668-590-01 [13668059001]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-03 [13668059003]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-06 [13668059006]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-02 [13668059002]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-30 [13668059030]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-25 [13668059025]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-04 [13668059004]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

NDC 13668-590-05 [13668059005]

Cetirizine Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA079191
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-04-15
Marketing End Date2010-04-15

Drug Details

Active Ingredients

IngredientStrength
CETIRIZINE HYDROCHLORIDE5 mg/1

OpenFDA Data

SPL SET ID:e4d24a50-cf09-4338-b286-af2721d22b9d
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014676

    • NDC Crossover Matching brand name "Cetirizine Hydrochloride" or generic name "Cetirizine Hydrochloride"

    NDCBrand NameGeneric Name
    0121-4780Cetirizine HydrochlorideCetirizine Hydrochloride
    0179-8301Cetirizine HydrochlorideCetirizine Hydrochloride
    0179-8302Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-0471Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-9899Cetirizine HydrochlorideCetirizine Hydrochloride
    0378-3635Cetirizine Hydrochloridecetirizine hydrochloride
    67668-161Cetirizine HydrochlorideCetirizine Hydrochloride
    67668-162Cetirizine HydrochlorideCetirizine Hydrochloride
    68016-353Cetirizine HydrochlorideCetirizine Hydrochloride
    68016-939Cetirizine HydrochlorideCetirizine Hydrochloride
    68071-1964Cetirizine HydrochlorideCetirizine Hydrochloride
    68071-1988Cetirizine HydrochlorideCetirizine Hydrochloride
    68151-1008Cetirizine HydrochlorideCetirizine Hydrochloride
    68151-3708Cetirizine HydrochlorideCetirizine Hydrochloride
    68788-0790Cetirizine HydrochlorideCetirizine Hydrochloride
    68788-6905Cetirizine HydrochlorideCetirizine Hydrochloride
    68788-9493Cetirizine HydrochlorideCetirizine Hydrochloride
    68788-9734Cetirizine HydrochlorideCetirizine Hydrochloride
    68788-9985Cetirizine hydrochlorideCetirizine hydrochloride
    68998-939Cetirizine HydrochlorideCetirizine Hydrochloride
    0536-1041Cetirizine HydrochlorideCetirizine Hydrochloride
    0536-4088Cetirizine HydrochlorideCetirizine Hydrochloride
    70518-0182Cetirizine HydrochlorideCetirizine Hydrochloride
    70518-0664Cetirizine HydrochlorideCetirizine Hydrochloride
    70518-0777Cetirizine HydrochlorideCetirizine Hydrochloride
    70518-0910Cetirizine HydrochlorideCetirizine Hydrochloride
    70518-1989Cetirizine HydrochlorideCetirizine Hydrochloride
    70985-002Cetirizine HydrochlorideCetirizine Hydrochloride
    71141-133Cetirizine HydrochlorideCetirizine Hydrochloride
    70934-199Cetirizine HydrochlorideCetirizine Hydrochloride
    71141-000Cetirizine HydrochlorideCetirizine Hydrochloride
    71205-164Cetirizine HydrochlorideCetirizine Hydrochloride
    70985-001Cetirizine HydrochlorideCetirizine Hydrochloride
    71205-207cetirizine hydrochloridecetirizine hydrochloride
    71335-0028Cetirizine HydrochlorideCetirizine Hydrochloride
    71335-0300Cetirizine HydrochlorideCetirizine Hydrochloride
    71205-093Cetirizine HydrochlorideCetirizine Hydrochloride
    71335-0755Cetirizine HydrochlorideCetirizine Hydrochloride
    71610-048CETIRIZINE HYDROCHLORIDECETIRIZINE HYDROCHLORIDE
    71610-093Cetirizine HydrochlorideCetirizine Hydrochloride
    0615-8240cetirizine hydrochloridecetirizine hydrochloride
    0781-1684Cetirizine HydrochlorideCetirizine Hydrochloride
    0781-1683Cetirizine HydrochlorideCetirizine Hydrochloride
    0781-5284Cetirizine HydrochlorideCetirizine Hydrochloride
    0781-5283Cetirizine HydrochlorideCetirizine Hydrochloride
    0904-5852Cetirizine HydrochlorideCetirizine Hydrochloride
    0904-5879Cetirizine HydrochlorideCetirizine Hydrochloride
    0904-6100Cetirizine hydrochlorideCetirizine hydrochloride
    10544-670Cetirizine HydrochlorideCetirizine Hydrochloride
    12634-987CETIRIZINE HYDROCHLORIDECETIRIZINE HYDROCHLORIDE
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