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    NDC 60219-2034-05 Carbidopa and Levodopa 50; 200 mg/1; mg/1 Details

    Carbidopa and Levodopa 50; 200 mg/1; mg/1

    Carbidopa and Levodopa is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is CARBIDOPA; LEVODOPA.

    Product Information

    NDC 60219-2034
    Product ID 60219-2034_3979736e-dac3-41a1-a3d7-d17b593a56da
    Associated GPIs
    GCN Sequence Number 016043
    GCN Sequence Number Description carbidopa/levodopa TABLET ER 50MG-200MG ORAL
    HIC3 H6A
    HIC3 Description ANTIPARKINSONISM DRUGS,OTHER
    GCN 62591
    HICL Sequence Number 013894
    HICL Sequence Number Description CARBIDOPA/LEVODOPA
    Brand/Generic Generic
    Proprietary Name Carbidopa and Levodopa
    Proprietary Name Suffix n/a
    Non-Proprietary Name CARBIDOPA and LEVODOPA
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 50; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name CARBIDOPA; LEVODOPA
    Labeler Name Amneal Pharmaceuticals NY LLC
    Pharmaceutical Class Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076521
    Listing Certified Through 2024-12-31

    Package

    NDC 60219-2034-05 (60219203405)

    NDC Package Code 60219-2034-5
    Billing NDC 60219203405
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (60219-2034-5)
    Marketing Start Date 2022-12-21
    NDC Exclude Flag N
    Pricing Information N/A