Search by Drug Name or NDC

    NDC 63629-2215-01 Labetalol HCL 300 mg/1 Details

    Labetalol HCL 300 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 63629-2215
    Product ID 63629-2215_02ac6586-8edb-5b91-e063-6394a90ad988
    Associated GPIs 33300010100315
    GCN Sequence Number 005100
    GCN Sequence Number Description labetalol HCl TABLET 300 MG ORAL
    HIC3 J7A
    HIC3 Description ALPHA/BETA-ADRENERGIC BLOCKING AGENTS
    GCN 10340
    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 300
    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 63629-2215-01 (63629221501)

    NDC Package Code 63629-2215-1
    Billing NDC 63629221501
    Package 100 TABLET, FILM COATED in 1 BOTTLE (63629-2215-1)
    Marketing Start Date 2021-02-08
    NDC Exclude Flag N
    Pricing Information N/A