NDC 51672-1280 – Desonide

Desonide .5 mg/g · Cream · Topical

Human Prescription Drug

Product NDC51672-1280

Product details

Brand name
Desonide
Generic name
Desonide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA073548
Marketed since
June 30, 1992
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Desonide →

Package NDC codes (2)

Package NDCDescriptionSince
51672-1280-11 TUBE in 1 CARTON (51672-1280-1) / 15 g in 1 TUBEJun 30, 1992
51672-1280-31 TUBE in 1 CARTON (51672-1280-3) / 60 g in 1 TUBEJun 30, 1992

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