NDC 71335-2813 – Hydroxychloroquine Sulfate

Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2813

Product details

Brand name
Hydroxychloroquine Sulfate
Generic name
Hydroxychloroquine sulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040150
Marketed since
May 8, 2025
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

Uses, dosage, side effects and warnings for Hydroxychloroquine Sulfate →

Package NDC codes (1)

Package NDCDescriptionSince
71335-2813-1100 TABLET in 1 BOTTLE (71335-2813-1)Oct 2, 2025

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