Label: ZYMAR- gatifloxacin solution/ drops

  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated April 19, 2018

If you are a consumer or patient please visit this version.

  • 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)