CYCLOSPORINE/CHONDROITIN PF (CYCLOSPORINE/CHONDROITIN SULFATE PF) EMULSION [IMPRIMIS NJOF, LLC]

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CYCLOSPORINE/CHONDROITIN PF (CYCLOSPORINE/CHONDROITIN SULFATE PF) EMULSION [IMPRIMIS NJOF, LLC]
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NDC 71384-514-05
Set ID 6ef02195-0ad6-0c27-e053-2991aa0aecb2
Category HUMAN PRESCRIPTION DRUG LABEL
Packager Imprimis NJOF, LLC
Generic Name
Product Class
Product Number
Application Number
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  • STORAGE AND HANDLING

    Store at 20° to 25° C (68° to 77° F)

  • PRINCIPAL DISPLAY PANEL

    Bottle Label

  • INGREDIENTS AND APPEARANCE
    CYCLOSPORINE/CHONDROITIN PF 
    cyclosporine/chondroitin sulfate pf emulsion
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:71384-514
    Route of AdministrationOPHTHALMIC
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CYCLOSPORINE (UNII: 83HN0GTJ6D) (CYCLOSPORINE - UNII:83HN0GTJ6D) CYCLOSPORINE1 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71384-514-055.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product07/01/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2018
    Labeler - Imprimis NJOF, LLC (080431967)
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