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    NDC 00781-3059-95 Digoxin 250 ug/mL Details

    Digoxin 250 ug/mL

    Digoxin is a INTRAMUSCULAR; INTRAVENOUS; PARENTERAL INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sandoz Inc. The primary component is DIGOXIN.

    Product Information

    NDC 00781-3059
    Product ID 0781-3059_27614ed2-aab9-4ceb-a780-36f0e84f186b
    Associated GPIs 31200010002010
    GCN Sequence Number 000015
    GCN Sequence Number Description digoxin AMPUL 250 MCG/ML INJECTION
    HIC3 A1A
    HIC3 Description DIGITALIS GLYCOSIDES
    GCN 00101
    HICL Sequence Number 000004
    HICL Sequence Number Description DIGOXIN
    Brand/Generic Generic
    Proprietary Name Digoxin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Digoxin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route INTRAMUSCULAR; INTRAVENOUS; PARENTERAL
    Active Ingredient Strength 250
    Active Ingredient Units ug/mL
    Substance Name DIGOXIN
    Labeler Name Sandoz Inc
    Pharmaceutical Class Cardiac Glycoside [EPC], Cardiac Glycosides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040481
    Listing Certified Through 2024-12-31

    Package

    NDC 00781-3059-95 (00781305995)

    NDC Package Code 0781-3059-95
    Billing NDC 00781305995
    Package 10 AMPULE in 1 CARTON (0781-3059-95) / 2 mL in 1 AMPULE (0781-3059-72)
    Marketing Start Date 2003-08-21
    NDC Exclude Flag N
    Pricing Information N/A