Cyclosporine/Chondroitin PF is a Ophthalmic Emulsion in the Human Prescription Drug category. It is labeled and distributed by Imprimis Njof, Llc. The primary component is Cyclosporine.
Product ID | 71384-514_6ef02195-0ad7-0c27-e053-2991aa0aecb2 |
NDC | 71384-514 |
Product Type | Human Prescription Drug |
Proprietary Name | Cyclosporine/Chondroitin PF |
Generic Name | Cyclosporine/chondroitin Sulfate Pf |
Dosage Form | Emulsion |
Route of Administration | OPHTHALMIC |
Marketing Start Date | 2018-07-01 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Imprimis NJOF, LLC |
Substance Name | CYCLOSPORINE |
Active Ingredient Strength | 1 mg/mL |
Pharm Classes | Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2018-07-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | ML |
Marketing Start Date | 2018-07-01 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-02-10 |
Ingredient | Strength |
---|---|
CYCLOSPORINE | 1 mg/mL |
SPL SET ID: | 6ef02195-0ad6-0c27-e053-2991aa0aecb2 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
71384-514 | Cyclosporine/Chondroitin PF | Cyclosporine/Chondroitin Sulfate PF |
70261-514 | Cyclosporine/Chondroitin Sulfate PF | Cyclosporine/Chondroitin Sulfate PF |