NDC 51672-1259 – Clobetasol Propionate

Clobetasol Propionate .5 mg/g · Ointment · Topical

Human Prescription Drug 2 recalls

Product NDC51672-1259

Product details

Brand name
Clobetasol Propionate
Generic name
Clobetasol Propionate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Ointment
Route
Topical
Marketing category
ANDA · ANDA074248
Marketed since
July 12, 1996
Listing expires
December 31, 2027
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Clobetasol Propionate →

Package NDC codes (4)

Package NDCDescriptionSince
51672-1259-11 TUBE in 1 CARTON (51672-1259-1) / 15 g in 1 TUBEJul 12, 1996
51672-1259-21 TUBE in 1 CARTON (51672-1259-2) / 30 g in 1 TUBEJul 12, 1996
51672-1259-31 TUBE in 1 CARTON (51672-1259-3) / 60 g in 1 TUBEJul 12, 1996
51672-1259-61 TUBE in 1 CARTON (51672-1259-6) / 45 g in 1 TUBEJul 12, 1996

Recalls mentioning this NDC

Other Clobetasol Propionate products