Label: CYCLOSPORINE/CHONDROITIN PF- cyclosporine/chondroitin sulfate pf emulsion
- NDC Code(s): 71384-514-05
- Packager: Imprimis NJOF, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Updated February 10, 2020
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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)