NDC 51672-2080 – Terbinafine Hydrochloride

Terbinafine Hydrochloride 1 g/100g · Cream · Topical

Human Otc Drug

Product NDC51672-2080

Product details

Brand name
Terbinafine Hydrochloride
Generic name
Terbinafine Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA077511
Marketed since
July 2, 2007
Listing expires
December 31, 2027
Pharmacologic class
Allylamine Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Terbinafine Hydrochloride →

Package NDC codes (7)

Package NDCDescriptionSince
51672-2080-11 TUBE in 1 CARTON (51672-2080-1) / 15 g in 1 TUBEJul 2, 2007
51672-2080-21 TUBE in 1 CARTON (51672-2080-2) / 30 g in 1 TUBEJul 2, 2007
51672-2080-31 TUBE in 1 CARTON (51672-2080-3) / 60 g in 1 TUBEJul 2, 2007
51672-2080-41 TUBE in 1 CARTON (51672-2080-4) / 15 g in 1 TUBEApr 24, 2017
51672-2080-61 TUBE in 1 CARTON (51672-2080-6) / 45 g in 1 TUBEJul 2, 2007
51672-2080-81 TUBE in 1 CARTON (51672-2080-8) / 12 g in 1 TUBEJul 2, 2007
51672-2080-91 TUBE in 1 CARTON (51672-2080-9) / 24 g in 1 TUBEJul 2, 2007

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