Search by Drug Name or NDC

    NDC 00143-9515-25 DROPERIDOL 2.5 mg/mL Details

    DROPERIDOL 2.5 mg/mL

    DROPERIDOL is a INTRAMUSCULAR; INTRAVENOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Hikma Pharmaceuticals USA Inc.. The primary component is DROPERIDOL.

    Product Information

    NDC 00143-9515
    Product ID 0143-9515_a7e520ca-3213-4203-9a23-5295d82088e3
    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 DROPERIDOL
    Proprietary Name Suffix n/a
    Non-Proprietary Name DROPERIDOL
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/mL
    Substance Name DROPERIDOL
    Labeler Name Hikma Pharmaceuticals USA Inc.
    Pharmaceutical Class Dopamine D2 Antagonists [MoA], Dopamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208197
    Listing Certified Through 2024-12-31

    Package

    NDC 00143-9515-25 (00143951525)

    NDC Package Code 0143-9515-25
    Billing NDC 00143951525
    Package 25 VIAL in 1 CARTON (0143-9515-25) / 1 mL in 1 VIAL (0143-9515-01)
    Marketing Start Date 2022-06-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d89f33ac-8a6e-49e7-94fb-84e58aad65a8 Details

    Revised: 6/2022