NDC 70518-0004

Ranitidine Immediate release

Ranitidine

Ranitidine Immediate release is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Ranitidine Hydrochloride.

Product ID70518-0004_8145b866-4195-0fa5-e053-2991aa0a120c
NDC70518-0004
Product TypeHuman Prescription Drug
Proprietary NameRanitidine Immediate release
Generic NameRanitidine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-11-16
Marketing CategoryANDA / ANDA
Application NumberANDA205512
Labeler NameREMEDYREPACK INC.
Substance NameRANITIDINE HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesHistamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70518-0004-3

90 TABLET in 1 BOTTLE, PLASTIC (70518-0004-3)
Marketing Start Date2018-09-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70518-0004-4 [70518000404]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-11-20
Marketing End Date2020-03-31

NDC 70518-0004-2 [70518000402]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-06-27
Marketing End Date2020-03-31

NDC 70518-0004-1 [70518000401]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-01-03
Marketing End Date2020-03-31

NDC 70518-0004-3 [70518000403]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-09-11
Marketing End Date2020-03-31

NDC 70518-0004-0 [70518000400]

Ranitidine Immediate release TABLET
Marketing CategoryANDA
Application NumberANDA205512
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-11-16
Marketing End Date2020-03-31

Drug Details

Active Ingredients

IngredientStrength
RANITIDINE HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:5708e52f-4585-4ac6-b34a-42a38292c136
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 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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