NDC 51672-1279 – Fluocinonide

Fluocinonide .5 mg/g · Gel · Topical

Human Prescription Drug 2 recalls

Product NDC51672-1279

Product details

Brand name
Fluocinonide
Generic name
Fluocinonide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Gel
Route
Topical
Marketing category
ANDA · ANDA074935
Marketed since
July 29, 1997
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Fluocinonide →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1279-11 TUBE in 1 CARTON (51672-1279-1) / 15 g in 1 TUBEJul 29, 1997
51672-1279-21 TUBE in 1 CARTON (51672-1279-2) / 30 g in 1 TUBEJul 29, 1997
51672-1279-31 TUBE in 1 CARTON (51672-1279-3) / 60 g in 1 TUBEJul 29, 1997

Recalls mentioning this NDC

Other Fluocinonide products