NDC 71335-9677 – Terbinafine hydrochloride

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9677

Product details

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

Package NDCDescriptionSince
71335-9677-130 TABLET in 1 BOTTLE, PLASTIC (71335-9677-1)Jun 6, 2023
71335-9677-260 TABLET in 1 BOTTLE, PLASTIC (71335-9677-2)Feb 3, 2025
71335-9677-390 TABLET in 1 BOTTLE, PLASTIC (71335-9677-3)Aug 30, 2023
71335-9677-4100 TABLET in 1 BOTTLE, PLASTIC (71335-9677-4)Feb 3, 2025
71335-9677-57 TABLET in 1 BOTTLE, PLASTIC (71335-9677-5)Feb 3, 2025
71335-9677-640 TABLET in 1 BOTTLE, PLASTIC (71335-9677-6)Feb 3, 2025
71335-9677-745 TABLET in 1 BOTTLE, PLASTIC (71335-9677-7)Jun 26, 2023
71335-9677-814 TABLET in 1 BOTTLE, PLASTIC (71335-9677-8)May 10, 2023
71335-9677-928 TABLET in 1 BOTTLE, PLASTIC (71335-9677-9)May 10, 2023

Other Terbinafine Hydrochloride products