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    NDC 27437-0205-10 SUPRAX 200 mg/1 Details

    SUPRAX 200 mg/1

    SUPRAX is a ORAL TABLET, CHEWABLE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is CEFIXIME.

    Product Information

    NDC 27437-0205
    Product ID 27437-205_ddcc8926-f489-4ea1-93eb-e959ea8f2e1f
    Associated GPIs 02300060000530
    GCN Sequence Number 070123
    GCN Sequence Number Description cefixime TAB CHEW 200 MG ORAL
    HIC3 W1Y
    HIC3 Description CEPHALOSPORIN ANTIBIOTICS - 3RD GENERATION
    GCN 33446
    HICL Sequence Number 003999
    HICL Sequence Number Description CEFIXIME
    Brand/Generic Brand
    Proprietary Name SUPRAX
    Proprietary Name Suffix n/a
    Non-Proprietary Name cefixime
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, CHEWABLE
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name CEFIXIME
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065380
    Listing Certified Through 2024-12-31

    Package

    NDC 27437-0205-10 (27437020510)

    NDC Package Code 27437-205-10
    Billing NDC 27437020510
    Package 10 TABLET, CHEWABLE in 1 BOTTLE (27437-205-10)
    Marketing Start Date 2012-12-05
    NDC Exclude Flag N
    Pricing Information N/A