Ketoconazole Cream, 2%

Product NDC
72641-005
11-digit product format
726410005
Labeler code
72641
Product ID
72641-005_c923698f-ed5d-4b3a-b54f-649389063603
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ketoconazole Cream, 2%
Dosage form
CREAM
Route
TOPICAL
Labeler
Tasman Pharma Inc.
Application
ANDA215185
Marketing category
ANDA
Marketing start
2021-11-17
Marketing end
0000-00-00
Substance
KETOCONAZOLE
Active strength
20 mg/g
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
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
72641-005-15726410005151 TUBE in 1 CARTON (72641-005-15) > 15 g in 1 TUBE1 tube2021-11-170000-00-00NoNoCurrent
72641-005-30726410005301 TUBE in 1 CARTON (72641-005-30) > 30 g in 1 TUBE1 tube2021-11-170000-00-00NoNoCurrent
72641-005-60726410005601 TUBE in 1 CARTON (72641-005-60) > 60 g in 1 TUBE1 tube2021-11-170000-00-00NoNoCurrent