NDC 41250-891

acid relief

Ranitidine

acid relief is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Meijer Distribution Inc. The primary component is Ranitidine Hydr.

Product ID41250-891_59285602-0b64-428a-a167-0a66d5b17c21
NDC41250-891
Product TypeHuman Otc Drug
Proprietary Nameacid relief
Generic NameRanitidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-12-06
Marketing CategoryANDA / ANDA
Application NumberANDA091429
Labeler NameMeijer Distribution Inc
Substance NameRANITIDINE HYDR
Active Ingredient Strength150 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 41250-891-01

1 BOTTLE in 1 CARTON (41250-891-01) > 95 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2019-03-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 41250-891-56 [41250089156]

acid relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-28

NDC 41250-891-01 [41250089101]

acid relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-03-27

NDC 41250-891-71 [41250089171]

acid relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-01-08

NDC 41250-891-02 [41250089102]

acid relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-28

NDC 41250-891-09 [41250089109]

acid relief TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA091429
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-12-06

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:f89bbc77-31d8-49b4-b123-a82797d0dc1e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198191

    • NDC Crossover Matching brand name "acid relief" or generic name "Ranitidine"

    NDCBrand NameGeneric Name
    41250-891acid reliefacid relief
    55312-950acid reliefacid relief
    41250-252acid reliefacid relief
    41250-577Acid ReliefAcid Relief
    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
    11673-023up and up ranitidineRanitidine
    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

    Trademark Results [acid relief]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    ACID RELIEF
    ACID RELIEF
    78100441 not registered Dead/Abandoned
    Hornack, Janmarie
    2001-12-31
    © 2025 FDA.report
    This site is not affiliated with or endorsed by the FDA.