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    NDC 63629-2212-01 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 Bryant Ranch Prepack. The primary component is LABETALOL HYDROCHLORIDE.

    Product Information

    NDC 63629-2212
    Product ID 63629-2212_02ab23b0-333a-8ced-e063-6394a90a7530
    Associated GPIs 33300010100305
    GCN Sequence Number 005098
    GCN Sequence Number Description labetalol HCl TABLET 100 MG ORAL
    HIC3 J7A
    HIC3 Description ALPHA/BETA-ADRENERGIC BLOCKING AGENTS
    GCN 10342
    HICL Sequence Number 002095
    HICL Sequence Number Description LABETALOL HCL
    Brand/Generic Generic
    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 Bryant Ranch Prepack
    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 63629-2212-01 (63629221201)

    NDC Package Code 63629-2212-1
    Billing NDC 63629221201
    Package 100 TABLET, FILM COATED in 1 BOTTLE (63629-2212-1)
    Marketing Start Date 2021-02-08
    NDC Exclude Flag N
    Pricing Information N/A