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    NDC 62332-0514-20 Treprostinil 20 mg/20mL Details

    Treprostinil 20 mg/20mL

    Treprostinil is a INTRAVENOUS; SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is TREPROSTINIL.

    Product Information

    NDC 62332-0514
    Product ID 62332-514_9c2bd447-15e1-4687-957f-cdb07e38cea4
    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 Treprostinil
    Proprietary Name Suffix n/a
    Non-Proprietary Name Treprostinil
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAVENOUS; SUBCUTANEOUS
    Active Ingredient Strength 20
    Active Ingredient Units mg/20mL
    Substance Name TREPROSTINIL
    Labeler Name Alembic Pharmaceuticals Inc.
    Pharmaceutical Class Prostacycline Vasodilator [EPC], Prostaglandins I [CS], Vasodilation [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211574
    Listing Certified Through 2024-12-31

    Package

    NDC 62332-0514-20 (62332051420)

    NDC Package Code 62332-514-20
    Billing NDC 62332051420
    Package 1 VIAL in 1 CARTON (62332-514-20) / 20 mL in 1 VIAL
    Marketing Start Date 2021-02-11
    NDC Exclude Flag N
    Pricing Information N/A