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    NDC 43066-0090-25 PROCHLORPERAZINE EDISYLATE 5 mg/mL Details

    PROCHLORPERAZINE EDISYLATE 5 mg/mL

    PROCHLORPERAZINE EDISYLATE is a INTRAMUSCULAR; INTRAVENOUS INJECTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Baxter Healthcare Corporation. The primary component is PROCHLORPERAZINE EDISYLATE.

    Product Information

    NDC 43066-0090
    Product ID 43066-090_e913c559-48fc-42e7-b8d0-de083005171f
    Associated GPIs 59200055202010
    GCN Sequence Number 067700
    GCN Sequence Number Description prochlorperazine edisylate VIAL 10 MG/2 ML INJECTION
    HIC3 H6J
    HIC3 Description ANTIEMETIC/ANTIVERTIGO AGENTS
    GCN 30314
    HICL Sequence Number 001628
    HICL Sequence Number Description PROCHLORPERAZINE EDISYLATE
    Brand/Generic Generic
    Proprietary Name PROCHLORPERAZINE EDISYLATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name prochlorperazine edisylate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION
    Route INTRAMUSCULAR; INTRAVENOUS
    Active Ingredient Strength 5
    Active Ingredient Units mg/mL
    Substance Name PROCHLORPERAZINE EDISYLATE
    Labeler Name Baxter Healthcare Corporation
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214379
    Listing Certified Through 2024-12-31

    Package

    NDC 43066-0090-25 (43066009025)

    NDC Package Code 43066-090-25
    Billing NDC 43066009025
    Package 25 VIAL in 1 CARTON (43066-090-25) / 2 mL in 1 VIAL (43066-090-01)
    Marketing Start Date 2021-05-03
    NDC Exclude Flag N
    Pricing Information N/A