NDC 71335-0042

Ranitidine Immediate release

Ranitidine

Ranitidine Immediate release 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 ID71335-0042_2238b362-057c-4698-9225-344e1d2e9b9f
NDC71335-0042
Product TypeHuman Prescription Drug
Proprietary NameRanitidine Immediate release
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-08-29
Marketing CategoryANDA / ANDA
Application NumberANDA205512
Labeler NameBryant Ranch Prepack
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength300 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0042-1

30 TABLET in 1 BOTTLE (71335-0042-1)
Marketing Start Date2017-02-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0042-7 [71335004207]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-5 [71335004205]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-3 [71335004203]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-9 [71335004209]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-1 [71335004201]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-8 [71335004208]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-6 [71335004206]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-2 [71335004202]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

NDC 71335-0042-4 [71335004204]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-02-15

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE300 mg/1

OpenFDA Data

SPL SET ID:37f2a2ac-e9ee-4dfa-8719-8efd0b8c73c5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198193

    • Pharmacological Class

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

    NDC Crossover Matching brand name "Ranitidine Immediate release" or generic name "Ranitidine"

    NDCBrand NameGeneric Name
    70518-0004Ranitidine Immediate releaseRanitidine Immediate release
    70518-0017Ranitidine Immediate releaseRanitidine Immediate release
    70518-1043Ranitidine Immediate releaseRanitidine Immediate release
    70518-1952Ranitidine Immediate releaseRanitidine Immediate release
    71205-007Ranitidine Immediate releaseRanitidine Immediate release
    71335-0042Ranitidine Immediate releaseRanitidine Immediate release
    53002-1028Ranitidine Immediate releaseRanitidine Immediate release
    58118-0803Ranitidine Immediate releaseRanitidine Immediate release
    63187-855Ranitidine Immediate releaseRanitidine Immediate release
    64380-804Ranitidine Immediate releaseRanitidine Immediate release
    64380-803Ranitidine Immediate releaseRanitidine Immediate release
    70934-332Ranitidine Immediate releaseRanitidine Immediate release
    51407-244Ranitidine Immediate releaseRanitidine Immediate release
    51407-245Ranitidine Immediate releaseRanitidine Immediate release
    64380-937Ranitidine Immediate releaseRanitidine Immediate release
    64380-936Ranitidine Immediate releaseRanitidine Immediate release
    68788-7423Ranitidine Immediate releaseRanitidine Immediate release
    71610-359Ranitidine Immediate releaseRanitidine Immediate release
    71610-371Ranitidine Immediate releaseRanitidine Immediate release
    71610-378Ranitidine Immediate releaseRanitidine Immediate release
    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
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