CYCLOSPORINE/CHONDROITIN SULFATE PF- cyclosporine/chondroitin sulfate pf emulsion 
ImprimisRx NJ

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.

----------

Store at 20° to 25° C (68° to 77° F)

Bottle Label

CYCLOSPORINE/CHONDROITIN SULFATE PF 
cyclosporine/chondroitin sulfate pf emulsion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70261-514
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:70261-514-055.5 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product02/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/01/2018
Labeler - ImprimisRx NJ (931390178)

Revised: 2/2018
Document Id: 6623a4de-d95d-7aef-e053-2991aa0a9235
Set id: 6623a4de-d95c-7aef-e053-2991aa0a9235
Version: 1
Effective Time: 20180226
 
ImprimisRx NJ