ZYMAR (GATIFLOXACIN) SOLUTION/ DROPS [ALLERGAN, INC.]

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ZYMAR (GATIFLOXACIN) SOLUTION/ DROPS [ALLERGAN, INC.]
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NDC 0023-9218-05
Set ID a5b0725e-9b7e-426b-ab1c-fcca3b1972fd
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Allergan, Inc.
Generic Name
Product Class
Product Number
Application Number
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  • PRINCIPAL DISPLAY PANEL - 3 MG/ML CARTON LABEL

    Rx only

    ZYMARTM

    (gatifloxacin
    ophthalmic solution)
    0.3%

    5 mL STERILE

    ® ALLERGAN

    Rx only ZYMARTM (gatifloxacin ophthalmic solution) 0.3% 5 mL STERILE ® ALLERGAN

  • PRINCIPAL DISPLAY PANEL - 3 MG/ML CARTON LABEL

    ZYMAR®

    Gatifloxacino

    Solución estéril

    0.3%

    Caja con 1 frasco
    con 5mL

    ®ALLERGAN

    ZYMAR® Gatifloxacino Solución estéril 0.3% Caja con 1 frasco con 5mL ®ALLERGAN

  • PRINCIPAL DISPLAY PANEL - 3 MG/ML CARTON LABEL

    Rx only

    ZYMARTM

    (gatifloxacin
    ophthalmic solution)
    0.3%

    5 mL STERILE

    ALLERGANTM

    Rx only ZYMARTM (gatifloxacin ophthalmic solution) 0.3% 5 mL STERILE ALLERGANTM

  • PRINCIPAL DISPLAY PANEL - 3 MG/ML CARTON LABEL

    ZYMARTM

    (gatifloxacin
    ophthalmic solution)
    0.3%

    5 mL 

    Rx only sterile

    ®ALLERGAN

    ZYMARTM (gatifloxacin ophthalmic solution) 0.3% 5 mL Rx only sterile ®ALLERGAN

  • INGREDIENTS AND APPEARANCE
    ZYMAR 
    gatifloxacin solution/ drops
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0023-9218
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GATIFLOXACIN (UNII: L4618BD7KJ) (GATIFLOXACIN ANHYDROUS - UNII:81485Y3A9A) GATIFLOXACIN3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0023-9218-051 in 1 CARTON04/11/2003
    15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    EXPORT ONLY04/11/2003
    Labeler - Allergan, Inc. (144796497)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allergan Sales, LLC362898611MANUFACTURE(0023-9218)
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