NDC 60687-909 – Terbinafine

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-909

Product details

Brand name
Terbinafine
Generic name
Terbinafine Hydrochloride
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078297
Marketed since
March 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Allylamine Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Terbinafine →

Package NDC codes (1)

Package NDCDescriptionSince
60687-909-2130 BLISTER PACK in 1 CARTON (60687-909-21) / 1 TABLET in 1 BLISTER PACK (60687-909-11)Mar 1, 2026

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