Search by Drug Name or NDC

    NDC 63629-7979-01 Flecainide Acetate 50 mg/1 Details

    Flecainide Acetate 50 mg/1

    Flecainide Acetate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is FLECAINIDE ACETATE.

    Product Information

    NDC 63629-7979
    Product ID 63629-7979_b56a83a2-c698-4384-93a5-887bbb6a384a
    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 Flecainide Acetate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Flecainide Acetate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name FLECAINIDE ACETATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Antiarrhythmic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202821
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-7979-01 (63629797901)

    NDC Package Code 63629-7979-1
    Billing NDC 63629797901
    Package 30 TABLET in 1 BOTTLE (63629-7979-1)
    Marketing Start Date 2021-12-23
    NDC Exclude Flag N
    Pricing Information N/A