CYCLOSPORINE/CHONDROITIN PF- cyclosporine/chondroitin sulfate pf emulsion

Cyclosporine/Chondroitin PF by

Drug Labeling and Warnings

Cyclosporine/Chondroitin PF by is a Prescription medication manufactured, distributed, or labeled by Imprimis NJOF, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

STORAGE AND HANDLING

Store at 20° to 25° C (68° to 77° F)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CYCLOSPORINE/CHONDROITIN PF 
cyclosporine/chondroitin sulfate pf emulsion

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 71384-514
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CYCLOSPORINE (UNII: 83HN0GTJ6D) (CYCLOSPORINE - UNII:83HN0GTJ6D)	CYCLOSPORINE	1 mg  in 1 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71384-514-05	5.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	07/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2018

Labeler - Imprimis NJOF, LLC (080431967)