NDC 69097-859 – Terbinafine

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-859

Product details

Brand name
Terbinafine
Generic name
Terbinafine
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077533
Marketed since
June 27, 2016
Listing expires
December 31, 2026
Pharmacologic class
Allylamine Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Terbinafine →

Package NDC codes (3)

Package NDCDescriptionSince
69097-859-0230 TABLET in 1 BOTTLE (69097-859-02)Jun 27, 2016
69097-859-07100 TABLET in 1 BOTTLE (69097-859-07)Jun 27, 2016
69097-859-12500 TABLET in 1 BOTTLE (69097-859-12)Jun 27, 2016

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