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    NDC 70518-3337-00 Diltiazem Hydrochloride 240 mg/1 Details

    Diltiazem Hydrochloride 240 mg/1

    Diltiazem Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is DILTIAZEM HYDROCHLORIDE.

    Product Information

    NDC 70518-3337
    Product ID 70518-3337_d80f12c8-0d5e-322a-e053-2995a90a56d9
    Associated GPIs
    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 Diltiazem Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Diltiazem hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 240
    Active Ingredient Units mg/1
    Substance Name DILTIAZEM HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205231
    Listing Certified Through 2023-12-31

    Package

    NDC 70518-3337-00 (70518333700)

    NDC Package Code 70518-3337-0
    Billing NDC 70518333700
    Package 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3337-0)
    Marketing Start Date 2022-01-20
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL cf864610-7636-43cc-a8ec-344afc1dc60e Details

    Revised: 2/2022