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    NDC 44087-3344-01 REBIF REBIDOSE 44 ug/.5mL Details

    REBIF REBIDOSE 44 ug/.5mL

    REBIF REBIDOSE is a SUBCUTANEOUS INJECTION, SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by EMD Serono, Inc.. The primary component is INTERFERON BETA-1A.

    Product Information

    NDC 44087-3344
    Product ID 44087-3344_348c7db6-5713-4329-83ca-14925b9b1d69
    Associated GPIs 6240306045D540
    GCN Sequence Number 070588
    GCN Sequence Number Description interferon beta-1a/albumin PEN INJCTR 44MCG/.5ML SUBCUT
    HIC3 H0E
    HIC3 Description AGENTS TO TREAT MULTIPLE SCLEROSIS
    GCN 34168
    HICL Sequence Number 023353
    HICL Sequence Number Description INTERFERON BETA-1A/ALBUMIN HUMAN
    Brand/Generic Brand
    Proprietary Name REBIF REBIDOSE
    Proprietary Name Suffix n/a
    Non-Proprietary Name INTERFERON BETA-1A
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION
    Route SUBCUTANEOUS
    Active Ingredient Strength 44
    Active Ingredient Units ug/.5mL
    Substance Name INTERFERON BETA-1A
    Labeler Name EMD Serono, Inc.
    Pharmaceutical Class Interferon beta [EPC], Interferon-beta [CS]
    DEA Schedule n/a
    Marketing Category BLA
    Application Number BLA103780
    Listing Certified Through 2024-12-31

    Package

    NDC 44087-3344-01 (44087334401)

    NDC Package Code 44087-3344-1
    Billing NDC 44087334401
    Package 12 PACKAGE in 1 CARTON (44087-3344-1) / .5 mL in 1 PACKAGE (44087-3344-9)
    Marketing Start Date 2012-12-21
    NDC Exclude Flag N
    Pricing Information N/A