NDC 70710-1157 – Leflunomide

Leflunomide 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70710-1157

Product details

Brand name
Leflunomide
Generic name
Leflunomide
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212308
Marketed since
April 26, 2019
Listing expires
December 31, 2026
Pharmacologic class
Antirheumatic Agent

Active ingredients

Uses, dosage, side effects and warnings for Leflunomide →

Package NDC codes (3)

Package NDCDescriptionSince
70710-1157-1100 TABLET, FILM COATED in 1 BOTTLE (70710-1157-1)Apr 26, 2019
70710-1157-330 TABLET, FILM COATED in 1 BOTTLE (70710-1157-3)Apr 26, 2019
70710-1157-5500 TABLET, FILM COATED in 1 BOTTLE (70710-1157-5)Apr 26, 2019

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