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    NDC 70518-3256-00 PROPOFOL 10 mg/mL Details

    PROPOFOL 10 mg/mL

    PROPOFOL is a INTRAVENOUS INJECTION, EMULSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is PROPOFOL.

    Product Information

    NDC 70518-3256
    Product ID 70518-3256_f7942a59-8cb9-193f-e053-6394a90a185e
    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 PROPOFOL
    Proprietary Name Suffix n/a
    Non-Proprietary Name PROPOFOL
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, EMULSION
    Route INTRAVENOUS
    Active Ingredient Strength 10
    Active Ingredient Units mg/mL
    Substance Name PROPOFOL
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class General Anesthesia [PE], General Anesthetic [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074848
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3256-00 (70518325600)

    NDC Package Code 70518-3256-0
    Billing NDC 70518325600
    Package 10 VIAL, SINGLE-USE in 1 CARTON (70518-3256-0) / 20 mL in 1 VIAL, SINGLE-USE
    Marketing Start Date 2021-10-25
    NDC Exclude Flag N
    Pricing Information N/A