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    NDC 76045-0213-20 Metoclopramide 10 mg/2mL Details

    Metoclopramide 10 mg/2mL

    Metoclopramide is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Fresenius Kabi USA, LLC. The primary component is METOCLOPRAMIDE HYDROCHLORIDE.

    Product Information

    NDC 76045-0213
    Product ID 76045-213_4a411ded-d608-41d3-bb26-67d5d5d3c9b5
    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 Metoclopramide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Metoclopramide Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 10
    Active Ingredient Units mg/2mL
    Substance Name METOCLOPRAMIDE HYDROCHLORIDE
    Labeler Name Fresenius Kabi USA, LLC
    Pharmaceutical Class Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091392
    Listing Certified Through 2024-12-31

    Package

    NDC 76045-0213-20 (76045021320)

    NDC Package Code 76045-213-20
    Billing NDC 76045021320
    Package 24 BLISTER PACK in 1 CARTON (76045-213-20) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-213-00) / 2 mL in 1 SYRINGE, GLASS
    Marketing Start Date 2022-02-28
    NDC Exclude Flag N
    Pricing Information N/A