NDC 72789-394 – Terbinafine

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72789-394

Product details

Brand name
Terbinafine
Generic name
Terbinafine Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
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
72789-394-4242 TABLET in 1 BOTTLE, PLASTIC (72789-394-42)Aug 5, 2024
72789-394-9090 TABLET in 1 BOTTLE, PLASTIC (72789-394-90)Apr 16, 2024

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