NDC 51672-1281 – Desonide

Desonide .5 mg/g · Ointment · Topical

Human Prescription Drug

Product NDC51672-1281

Product details

Brand name
Desonide
Generic name
Desonide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Ointment
Route
Topical
Marketing category
ANDA · ANDA074254
Marketed since
August 3, 1994
Listing expires
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Desonide →

Package NDC codes (2)

Package NDCDescriptionSince
51672-1281-11 TUBE in 1 CARTON (51672-1281-1) / 15 g in 1 TUBEAug 3, 1994
51672-1281-31 TUBE in 1 CARTON (51672-1281-3) / 60 g in 1 TUBEAug 3, 1994

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