Desoximetasone

Product NDC
0168-0180
11-digit product format
001680180
Labeler code
0168
Product ID
0168-0180_3e7ef6cc-659b-4f69-ac46-905fa237d2e8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desoximetasone
Dosage form
CREAM
Route
TOPICAL
Labeler
E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.
Application
ANDA078369
Marketing category
ANDA
Marketing start
2010-06-29
Marketing end
0000-00-00
Substance
DESOXIMETASONE
Active strength
3 mg/g
Pharmacologic classes
Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0168-0180-15001680180151 TUBE in 1 CARTON (0168-0180-15) > 15 g in 1 TUBE1 tube2010-06-290000-00-00NoNoCurrent
0168-0180-60001680180601 TUBE in 1 CARTON (0168-0180-60) > 60 g in 1 TUBE1 tube2010-06-290000-00-00NoNoCurrent
0168-0180-99001680180991 TUBE in 1 CARTON (0168-0180-99) > 100 g in 1 TUBE1 tube2010-06-290000-00-00NoNoCurrent