Ketoconazole

Product NDC
72162-1409
11-digit product format
721621409
Labeler code
72162
Product ID
72162-1409_5f62607f-1eda-4b69-a2a3-17986ea0686b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ketoconazole
Dosage form
SHAMPOO, SUSPENSION
Route
TOPICAL
Labeler
Bryant Ranch Prepack
Application
ANDA076419
Marketing category
ANDA
Marketing start
2010-01-19
Substance
KETOCONAZOLE
Active strength
20 mg/mL
Pharmacologic classes
Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein 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
R9400W927IKETOCONAZOLE65277-42-1KETOCONAZOLE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1409-272162140902120 mL in 1 BOTTLE (72162-1409-2) 120 ml2024-06-20NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ketoconazole Shampoo, 2%Bryant Ranch Prepack2024-06-20HUMAN PRESCRIPTION DRUG LABEL1