NDC 16714-795 – Terbinafine

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC16714-795

Product details

Brand name
Terbinafine
Generic name
Terbinafine Hydrochloride
Labeler
NorthStar Rx LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078297
Marketed since
July 2, 2007
Listing expires
December 31, 2026
Pharmacologic class
Allylamine Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Terbinafine →

Package NDC codes (2)

Package NDCDescriptionSince
16714-795-0130 TABLET in 1 BOTTLE (16714-795-01)Jul 2, 2007
16714-795-02100 TABLET in 1 BOTTLE (16714-795-02)Jul 2, 2007

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