NDC 71335-2256 – Leflunomide

Leflunomide 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2256

Product details

Brand name
Leflunomide
Generic name
Leflunomide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213652
Marketed since
March 29, 2021
Listing expires
December 31, 2026
Pharmacologic class
Antirheumatic Agent

Active ingredients

Uses, dosage, side effects and warnings for Leflunomide →

Package NDC codes (2)

Package NDCDescriptionSince
71335-2256-130 TABLET, FILM COATED in 1 BOTTLE (71335-2256-1)Sep 25, 2023
71335-2256-290 TABLET, FILM COATED in 1 BOTTLE (71335-2256-2)Sep 6, 2024

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