MedPath

Ciclopirox

Prescribing information

Approved
Approval ID

aaa27021-68a6-486c-9095-56de1140ca2d

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Mar 21, 2024

Manufacturers
FDA

Bryant Ranch Prepack

DUNS: 171714327

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Ciclopirox

PRODUCT DETAILS

NDC Product Code72162-1321
Application NumberANDA078172
Marketing CategoryC73584
Route of AdministrationTOPICAL
Effective DateMarch 21, 2024
Generic NameCiclopirox

INGREDIENTS (3)

ETHYL ACETATEInactive
Code: 76845O8NMZ
Classification: IACT
CICLOPIROXActive
Quantity: 80 mg in 1 mL
Code: 19W019ZDRJ
Classification: ACTIB
ISOPROPYL ALCOHOLInactive
Code: ND2M416302
Classification: IACT

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Ciclopirox - FDA Drug Approval Details