Search by Drug Name or NDC

    NDC 70518-1546-00 Labetalol HCL 100 mg/1 Details

    Labetalol HCL 100 mg/1

    Labetalol HCL is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is LABETALOL HYDROCHLORIDE.

    Product Information

    NDC 70518-1546
    Product ID 70518-1546_fa3f7bb7-e8e3-bec3-e053-6394a90af965
    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 Labetalol HCL
    Proprietary Name Suffix n/a
    Non-Proprietary Name Labetalol Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name LABETALOL HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA200908
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1546-00 (70518154600)

    NDC Package Code 70518-1546-0
    Billing NDC 70518154600
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1546-0)
    Marketing Start Date 2018-10-17
    NDC Exclude Flag N
    Pricing Information N/A