CICLOPIROX

Product NDC
72162-1126
11-digit product format
721621126
Labeler code
72162
Product ID
72162-1126_fdda6ce3-b610-4510-95fc-0df24f9e5903
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
CICLOPIROX
Dosage form
GEL
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA078266
Marketing category
ANDA
Marketing start
2009-01-07
Substance
CICLOPIROX
Active strength
7.7 mg/g
Pharmacologic classes
Decreased DNA Replication [PE], Decreased Protein Synthesis [PE], Decreased RNA Replication [PE], Protein Synthesis Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
19W019ZDRJCICLOPIROX29342-05-0CICLOPIROX

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1126-1721621126011 TUBE in 1 CARTON (72162-1126-1) / 100 g in 1 TUBE1 tube2024-03-11NoNoHistorical
72162-1126-2721621126021 TUBE in 1 CARTON (72162-1126-2) / 45 g in 1 TUBE1 tube2024-03-11NoNoHistorical
72162-1126-3721621126031 TUBE in 1 CARTON (72162-1126-3) / 30 g in 1 TUBE1 tube2024-03-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ciclopirox Gel, 0.77%Bryant Ranch Prepack2025-09-16HUMAN PRESCRIPTION DRUG LABEL101