NDC 58602-733

RANITIDINE

Ranitidine

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

Product ID58602-733_8f1b503c-2663-45a1-b9f6-c951509f6958
NDC58602-733
Product TypeHuman Otc Drug
Proprietary NameRANITIDINE
Generic NameRanitidine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-11-13
Marketing CategoryANDA / ANDA
Application NumberANDA207579
Labeler NameAurohealth LLC
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength75 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58602-733-03

1 BLISTER PACK in 1 CARTON (58602-733-03) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2017-11-13
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58602-733-23 [58602073323]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-22 [58602073322]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-30 [58602073330]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-09 [58602073309]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-15 [58602073315]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-03 [58602073303]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-40 [58602073340]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

NDC 58602-733-18 [58602073318]

RANITIDINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA207579
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-13

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE75 mg/1

OpenFDA Data

SPL SET ID:65b08aa1-9742-4151-af53-ac1fe9478f4b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 312773

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

    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
    10544-056RanitidineRanitidine
    10544-438RanitidineRanitidine
    10544-516RanitidineRanitidine
    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
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