NDC 51672-1298 – Ketoconazole

Ketoconazole 20 mg/g · Cream · Topical

Human Prescription Drug

Product NDC51672-1298

Product details

Brand name
Ketoconazole
Generic name
Ketoconazole
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA075638
Marketed since
December 18, 2002
Listing expires
December 31, 2026
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Ketoconazole →

Package NDC codes (3)

Package NDCDescriptionSince
51672-1298-11 TUBE in 1 CARTON (51672-1298-1) / 15 g in 1 TUBEDec 18, 2002
51672-1298-21 TUBE in 1 CARTON (51672-1298-2) / 30 g in 1 TUBEDec 18, 2002
51672-1298-31 TUBE in 1 CARTON (51672-1298-3) / 60 g in 1 TUBEDec 18, 2002

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