NDC 53746-254

Ranitidine

Ranitidine

Ranitidine is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Amneal Pharmaceuticals Of New York Llc. The primary component is Ranitidine Hydrochloride.

Product ID53746-254_264352d0-df37-44c9-9cb4-c9fff8270f71
NDC53746-254
Product TypeHuman Prescription Drug
Proprietary NameRanitidine
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-12-16
Marketing CategoryANDA / ANDA
Application NumberANDA077824
Labeler NameAmneal Pharmaceuticals of New York LLC
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength300 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 53746-254-01

100 TABLET in 1 BOTTLE (53746-254-01)
Marketing Start Date2009-12-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 53746-254-01 [53746025401]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-16

NDC 53746-254-05 [53746025405]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-16
Marketing End Date2015-11-10

NDC 53746-254-24 [53746025424]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-16
Marketing End Date2015-03-09

NDC 53746-254-02 [53746025402]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-16

NDC 53746-254-30 [53746025430]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-12-16

NDC 53746-254-10 [53746025410]

Ranitidine TABLET
Marketing CategoryANDA
Application NumberANDA077824
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-12-16
Marketing End Date2015-11-10

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE300 mg/1

OpenFDA Data

SPL SET ID:b38a3332-5c54-453f-aeb7-070f830955c2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198193
  • 198191
    • UPC Code
  • 0353746253019
  • 0353746254016

    • Pharmacological Class

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

    Medicade Reported Pricing

    53746025430 RANITIDINE 300 MG TABLET

    Pricing Unit: EA | Drug Type:

    53746025402 RANITIDINE 300 MG TABLET

    Pricing Unit: EA | Drug Type:

    53746025401 RANITIDINE 300 MG TABLET

    Pricing Unit: EA | Drug Type:

    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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