Cyclosporine/Chondroitin Sulfate PF
Approved
Approval ID
6623a4de-d95c-7aef-e053-2991aa0a9235
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 26, 2018
Manufacturers
FDA
ImprimisRx NJ
DUNS: 931390178
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 Code70261-514
Product Classification
G
Generic Name
Cyclosporine/Chondroitin Sulfate PF
Product Specifications
Route of AdministrationOPHTHALMIC
Effective DateFebruary 26, 2018
FDA Product Classification
INGREDIENTS (1)
CYCLOSPORINEActive
Quantity: 1 mg in 1 mL
Code: 83HN0GTJ6D
Classification: ACTIB