Drug Labeling and Warnings

Drug Details

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CYCLOSPORINE/CHONDROITIN PF- cyclosporine/chondroitin sulfate pf emulsion 
Imprimis NJOF, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Store at 20° to 25° C (68° to 77° F)

Bottle Label

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)

Revised: 6/2018
 
Imprimis NJOF, LLC


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