NDC 71335-0394

Ranitidine

Ranitidine

Ranitidine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Ranitidine Hydrochloride.

Product ID71335-0394_4076d8d3-f6f9-465d-beda-ff7c9dffdb86
NDC71335-0394
Product TypeHuman Prescription Drug
Proprietary NameRanitidine
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-16
Marketing CategoryANDA / ANDA
Application NumberANDA077824
Labeler NameBryant Ranch Prepack
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 71335-0394-0

10 TABLET in 1 BOTTLE (71335-0394-0)
Marketing Start Date2018-05-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0394-8 [71335039408]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-5 [71335039405]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-3 [71335039403]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-2 [71335039402]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-4 [71335039404]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-9 [71335039409]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-0 [71335039400]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-7 [71335039407]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-1 [71335039401]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

NDC 71335-0394-6 [71335039406]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-12-07

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:4076d8d3-f6f9-465d-beda-ff7c9dffdb86
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198191

    • Pharmacological Class

    • Histamine H2 Receptor Antagonists [MoA]
    • Histamine-2 Receptor Antagonist [EPC]

    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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