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    NDC 70518-0033-00 ALENDRONATE SODIUM 70 mg/1 Details

    ALENDRONATE SODIUM 70 mg/1

    ALENDRONATE SODIUM is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is ALENDRONATE SODIUM.

    Product Information

    NDC 70518-0033
    Product ID 70518-0033_0e0d0262-2610-7ffe-e063-6394a90a48b4
    Associated GPIs 30042010100370
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name ALENDRONATE SODIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Alendronate sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 70
    Active Ingredient Units mg/1
    Substance Name ALENDRONATE SODIUM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Bisphosphonate [EPC], Diphosphonates [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076768
    Listing Certified Through 2025-12-31

    Package

    NDC 70518-0033-00 (70518003300)

    NDC Package Code 70518-0033-0
    Billing NDC 70518003300
    Package 12 TABLET in 1 BLISTER PACK (70518-0033-0)
    Marketing Start Date 2016-12-01
    NDC Exclude Flag N
    Pricing Information N/A