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    NDC 25021-0790-02 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 Sagent Pharmaceuticals. The primary component is PROCHLORPERAZINE EDISYLATE.

    Product Information

    NDC 25021-0790
    Product ID 25021-790_18174b35-89ba-487a-bbc5-95716b8c1274
    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 Sagent Pharmaceuticals
    Pharmaceutical Class Phenothiazine [EPC], Phenothiazines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214107
    Listing Certified Through 2024-12-31

    Package

    NDC 25021-0790-02 (25021079002)

    NDC Package Code 25021-790-02
    Billing NDC 25021079002
    Package 10 VIAL in 1 CARTON (25021-790-02) / 2 mL in 1 VIAL
    Marketing Start Date 2021-11-15
    NDC Exclude Flag N
    Pricing Information N/A