NDC 51672-1264 – Fluocinonide

Fluocinonide .5 mg/g · Ointment · Topical

Human Prescription Drug 2 recalls

Product NDC51672-1264

Product details

Brand name
Fluocinonide
Generic name
Fluocinonide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Ointment
Route
Topical
Marketing category
ANDA · ANDA075008
Marketed since
June 30, 1999
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Fluocinonide →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1264-11 TUBE in 1 CARTON (51672-1264-1) / 15 g in 1 TUBEJun 30, 1999
51672-1264-21 TUBE in 1 CARTON (51672-1264-2) / 30 g in 1 TUBEJun 30, 1999
51672-1264-31 TUBE in 1 CARTON (51672-1264-3) / 60 g in 1 TUBEJun 30, 1999

Recalls mentioning this NDC

Other Fluocinonide products