Search by Drug Name or NDC

    NDC 62135-0321-90 Methyldopa 250 mg/1 Details

    Methyldopa 250 mg/1

    Methyldopa is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Chartwell RX, LLC. The primary component is METHYLDOPA.

    Product Information

    NDC 62135-0321
    Product ID 62135-321_f174f4ef-f4e1-315d-e053-2a95a90a85a6
    Associated GPIs
    GCN Sequence Number 000361
    GCN Sequence Number Description methyldopa TABLET 250 MG ORAL
    HIC3 A4B
    HIC3 Description ANTIHYPERTENSIVES, SYMPATHOLYTIC
    GCN 01431
    HICL Sequence Number 000118
    HICL Sequence Number Description METHYLDOPA
    Brand/Generic Generic
    Proprietary Name Methyldopa
    Proprietary Name Suffix n/a
    Non-Proprietary Name Methyldopa
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name METHYLDOPA
    Labeler Name Chartwell RX, LLC
    Pharmaceutical Class Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA018934
    Listing Certified Through 2024-12-31

    Package

    NDC 62135-0321-90 (62135032190)

    NDC Package Code 62135-321-90
    Billing NDC 62135032190
    Package 90 TABLET, FILM COATED in 1 BOTTLE (62135-321-90)
    Marketing Start Date 2022-11-22
    NDC Exclude Flag N
    Pricing Information N/A