NDC 51672-1261 – Desoximetasone

Desoximetasone .5 mg/g · Gel · Topical

Human Prescription Drug 2 recalls

Product NDC51672-1261

Product details

Brand name
Desoximetasone
Generic name
Desoximetasone
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Gel
Route
Topical
Marketing category
ANDA · ANDA074904
Marketed since
July 14, 1998
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Desoximetasone →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1261-11 TUBE in 1 CARTON (51672-1261-1) / 15 g in 1 TUBEJul 14, 1998
51672-1261-21 TUBE in 1 CARTON (51672-1261-2) / 30 g in 1 TUBEJul 14, 1998
51672-1261-31 TUBE in 1 CARTON (51672-1261-3) / 60 g in 1 TUBEJul 14, 1998

Recalls mentioning this NDC

Other Desoximetasone products