NDC 71335-1124 – Terbinafine

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1124

Product details

Brand name
Terbinafine
Generic name
Terbinafine Hydrochloride
Labeler
Bryant Ranch Prepack
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 (9)

Package NDCDescriptionSince
71335-1124-130 TABLET in 1 BOTTLE (71335-1124-1)Feb 26, 2019
71335-1124-260 TABLET in 1 BOTTLE (71335-1124-2)May 30, 2024
71335-1124-390 TABLET in 1 BOTTLE (71335-1124-3)Mar 1, 2021
71335-1124-4100 TABLET in 1 BOTTLE (71335-1124-4)May 30, 2024
71335-1124-57 TABLET in 1 BOTTLE (71335-1124-5)May 30, 2024
71335-1124-640 TABLET in 1 BOTTLE (71335-1124-6)May 30, 2024
71335-1124-745 TABLET in 1 BOTTLE (71335-1124-7)Feb 27, 2019
71335-1124-814 TABLET in 1 BOTTLE (71335-1124-8)Nov 14, 2019
71335-1124-928 TABLET in 1 BOTTLE (71335-1124-9)May 30, 2024

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