Cyclosporine/Chondroitin PF
Approved
Approval ID
6ef02195-0ad6-0c27-e053-2991aa0aecb2
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 10, 2020
Manufacturers
FDA
Imprimis NJOF, LLC
DUNS: 080431967
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Cyclosporine/Chondroitin Sulfate PF
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71384-514
Product Classification
G
Generic Name
Cyclosporine/Chondroitin Sulfate PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateFebruary 10, 2020
FDA Product Classification
INGREDIENTS (1)
CYCLOSPORINEActive
Quantity: 1 mg in 1 mL
Code: 83HN0GTJ6D
Classification: ACTIB