Search by Drug Name or NDC

    NDC 31722-0845-30 Moxifloxacin 400 mg/1 Details

    Moxifloxacin 400 mg/1

    Moxifloxacin is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Camber Pharmaceuticals, Inc.. The primary component is MOXIFLOXACIN HYDROCHLORIDE.

    Product Information

    NDC 31722-0845
    Product ID 31722-845_f6e9a43c-e301-ff1f-e053-6394a90a1458
    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 Moxifloxacin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Moxifloxacin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 400
    Active Ingredient Units mg/1
    Substance Name MOXIFLOXACIN HYDROCHLORIDE
    Labeler Name Camber Pharmaceuticals, Inc.
    Pharmaceutical Class Quinolone Antimicrobial [EPC], Quinolones [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204836
    Listing Certified Through 2024-12-31

    Package

    NDC 31722-0845-30 (31722084530)

    NDC Package Code 31722-845-30
    Billing NDC 31722084530
    Package 30 TABLET, FILM COATED in 1 BOTTLE (31722-845-30)
    Marketing Start Date 2023-03-02
    NDC Exclude Flag N
    Pricing Information N/A