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    NDC 63187-0169-06 Azithromycin 250 mg/1 Details

    Azithromycin 250 mg/1

    Azithromycin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is AZITHROMYCIN MONOHYDRATE.

    Product Information

    NDC 63187-0169
    Product ID 63187-169_9471b50f-3435-48b2-a04b-d18e4bca88dc
    Associated GPIs 03400010000320
    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 Azithromycin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Azithromycin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name AZITHROMYCIN MONOHYDRATE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Macrolide Antimicrobial [EPC], Macrolides [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065211
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0169-06 (63187016906)

    NDC Package Code 63187-169-06
    Billing NDC 63187016906
    Package 1 DOSE PACK in 1 CARTON (63187-169-06) / 6 TABLET, FILM COATED in 1 DOSE PACK
    Marketing Start Date 2014-09-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 1926be99-3b3e-45ff-a1b9-4eb31312dd57 Details

    Revised: 11/2019