NDC 11673-023

up and up ranitidine

Ranitidine

up and up ranitidine is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Target Corporation. The primary component is Ranitidine Hydrochloride.

Product ID11673-023_f35d68b6-4b55-49eb-8f1c-3cd8a68a4077
NDC11673-023
Product TypeHuman Otc Drug
Proprietary Nameup and up ranitidine
Generic NameRanitidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2015-04-01
Marketing CategoryANDA / ANDA
Application NumberANDA091429
Labeler NameTarget Corporation
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 11673-023-02

1 BOTTLE in 1 CARTON (11673-023-02) > 24 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2015-04-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11673-023-09 [11673002309]

up and up ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-04-01

NDC 11673-023-02 [11673002302]

up and up ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-04-01

NDC 11673-023-75 [11673002375]

up and up ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-08-23

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:5c5521ef-1c0a-4679-bacd-4c418ec02633
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198191

    • NDC Crossover Matching brand name "up and up ranitidine" or generic name "Ranitidine"

    NDCBrand NameGeneric Name
    11673-023up and up ranitidineRanitidine
    11673-876up and up ranitidineup and up ranitidine
    11673-852Up and Up RanitidineUp and Up Ranitidine
    10202-8527 Select Acid ReducerRanitidine
    0904-6350Acid ReducerRanitidine
    0113-7950basic care acid reducerRanitidine
    0113-7852basic care acid reducer 150Ranitidine
    0113-7876basic care acid reducer 75Ranitidine
    0113-0852Good Sense Acid ReducerRanitidine
    0113-0876Good Sense Acid ReducerRanitidine
    10202-712MAXIMUM STRENGTH RANITIDINERanitidine
    0597-0121Maximum Strength Zantacranitidine
    0121-0727RanitidineRANITIDINE
    0121-4727RanitidineRANITIDINE
    0172-4357RanitidineRanitidine
    0172-4358RanitidineRanitidine
    0363-0352RanitidineRanitidine
    0440-8300RanitidineRanitidine
    0440-8305RanitidineRanitidine
    0615-4513RanitidineRanitidine
    0615-4514RanitidineRanitidine
    0615-8021RanitidineRanitidine
    0781-6087RanitidineRanitidine
    0904-6349RanitidineRanitidine
    0904-6716RanitidineRanitidine
    0904-6921RanitidineRanitidine
    10544-056RanitidineRanitidine
    10544-438RanitidineRanitidine
    10544-516RanitidineRanitidine
    11673-849RanitidineRanitidine
    0904-6715ranitidine 75Ranitidine
    0363-0852wal zan 150Ranitidine
    0363-0950wal zan 150Ranitidine
    0363-1876wal zan 75Ranitidine
    0363-0362Wal-ZanRanitidine
    0597-0122Zantac 75ranitidine
    0597-0120Zantac Maximum Strength 150 Cool Mintranitidine
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.