NDC 71335-3142 – Hydroxychloroquine Sulfate

Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3142

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, 2027
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-3142-1100 TABLET in 1 BOTTLE (71335-3142-1)Jun 8, 2026
71335-3142-230 TABLET in 1 BOTTLE (71335-3142-2)Jun 8, 2026
71335-3142-360 TABLET in 1 BOTTLE (71335-3142-3)Jun 8, 2026
71335-3142-4180 TABLET in 1 BOTTLE (71335-3142-4)Jun 8, 2026
71335-3142-590 TABLET in 1 BOTTLE (71335-3142-5)Jun 8, 2026
71335-3142-6120 TABLET in 1 BOTTLE (71335-3142-6)Jun 8, 2026
71335-3142-710 TABLET in 1 BOTTLE (71335-3142-7)Jun 8, 2026
71335-3142-814 TABLET in 1 BOTTLE (71335-3142-8)Jun 8, 2026
71335-3142-920 TABLET in 1 BOTTLE (71335-3142-9)Jun 8, 2026

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