NDC 60505-4623

Ranitidine

Ranitidine Hydrochloride

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

Product ID60505-4623_79026753-b4f6-b094-f0f3-156492d41412
NDC60505-4623
Product TypeHuman Otc Drug
Proprietary NameRanitidine
Generic NameRanitidine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-07-27
Marketing End Date2020-10-31
Marketing CategoryANDA / ANDA
Application NumberANDA200172
Labeler NameApotex Corp.
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
NDC Exclude FlagN

Packaging

NDC 60505-4623-9

1 BOTTLE in 1 CARTON (60505-4623-9) > 90 TABLET, FILM COATED in 1 BOTTLE
Marketing Start Date2017-07-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60505-4623-5 [60505462305]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200172
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-07-27
Marketing End Date2020-10-31

NDC 60505-4623-6 [60505462306]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200172
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-07-27
Marketing End Date2020-10-31

NDC 60505-4623-2 [60505462302]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200172
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-07-27
Marketing End Date2019-10-31

NDC 60505-4623-8 [60505462308]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200172
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-07-27
Marketing End Date2020-10-31

NDC 60505-4623-9 [60505462309]

Ranitidine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA200172
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-07-27
Marketing End Date2020-10-31

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:b44ad5ae-28a9-3e44-c3a9-abde56308361
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198191

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

    NDCBrand NameGeneric Name
    0121-0727RanitidineRANITIDINE
    0121-4727RanitidineRANITIDINE
    0172-4357RanitidineRanitidine
    0172-4358RanitidineRanitidine
    0363-0352RanitidineRanitidine
    0440-2300RanitidineRanitidine Hydrochloride
    0440-8300RanitidineRanitidine
    0440-8305RanitidineRanitidine
    0615-4513RanitidineRanitidine
    0615-4514RanitidineRanitidine
    0615-8021RanitidineRanitidine
    0781-6087RanitidineRanitidine
    0904-6349RanitidineRanitidine
    0904-6716RanitidineRanitidine
    0904-6921RanitidineRanitidine
    68071-2190RanitidineRanitidine
    68071-3162RanitidineRanitidine
    68071-3317RanitidineRanitidine
    68071-2185RanitidineRanitidine
    68071-3248RanitidineRanitidine
    68071-3165RanitidineRanitidine
    68151-1610RanitidineRanitidine
    68151-2890RanitidineRanitidine
    68462-248RanitidineRanitidine
    68462-249RanitidineRanitidine
    68788-6382RanitidineRanitidine
    68788-7101RanitidineRanitidine
    68788-7078RanitidineRanitidine
    68788-7388RanitidineRanitidine
    68788-9875RanitidineRanitidine
    68788-9874RanitidineRanitidine
    70408-141RANITIDINERANITIDINE
    70518-0222RanitidineRanitidine
    70518-0263RanitidineRanitidine
    70518-0093RanitidineRanitidine
    70518-0622RanitidineRanitidine
    70518-0873RanitidineRanitidine
    70518-0801RanitidineRanitidine
    70518-1361RanitidineRanitidine
    70518-1714RanitidineRanitidine
    70934-017RanitidineRanitidine
    71141-013RanitidineRanitidine
    71335-0394RanitidineRanitidine
    71335-0342RanitidineRanitidine
    71335-0363RanitidineRanitidine
    71821-001RanitidineRanitidine
    71821-002RanitidineRanitidine
    10544-438RanitidineRanitidine
    10544-056RanitidineRanitidine
    10544-516RanitidineRanitidine
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