Cyclosporine

Product NDC

0185-0932

11-digit product format

001850932

Labeler code

0185

Product ID

0185-0932_6eeab0c7-3a33-4004-8782-d5b9e0f59abb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cyclosporine

Dosage form

CAPSULE

Route

ORAL

Labeler

Eon Labs, Inc.

Application

ANDA065017

Marketing category

ANDA

Marketing start

2000-01-13

Marketing end

2020-03-31

Substance

CYCLOSPORINE

Active strength

25 mg/1

Pharmacologic classes

Calcineurin Inhibitor Immunosuppressant [EPC],Calcineurin Inhibitors [MoA],Cytochrome P450 3A4 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record