NDC 69452-351 – Terbinafine hydrochloride

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69452-351

Product details

Brand name
Terbinafine hydrochloride
Generic name
Terbinafine hydrochloride
Labeler
Bionpharma Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078163
Marketed since
January 28, 2022
Listing expires
December 31, 2026
Pharmacologic class
Allylamine Antifungal

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
69452-351-1330 TABLET in 1 BOTTLE, PLASTIC (69452-351-13)Jan 28, 2022
69452-351-20100 TABLET in 1 BOTTLE, PLASTIC (69452-351-20)Jan 28, 2022

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