NDC 71335-3079 – Hydroxychloroquine Sulfate

Hydroxychloroquine Sulfate 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-3079

Product details

Brand name
Hydroxychloroquine Sulfate
Generic name
Hydroxychloroquine Sulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040766
Marketed since
June 3, 2024
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
71335-3079-1100 TABLET, FILM COATED in 1 BOTTLE (71335-3079-1)Feb 13, 2026
71335-3079-230 TABLET, FILM COATED in 1 BOTTLE (71335-3079-2)Feb 13, 2026
71335-3079-360 TABLET, FILM COATED in 1 BOTTLE (71335-3079-3)Feb 13, 2026
71335-3079-4180 TABLET, FILM COATED in 1 BOTTLE (71335-3079-4)Feb 13, 2026
71335-3079-590 TABLET, FILM COATED in 1 BOTTLE (71335-3079-5)Feb 13, 2026
71335-3079-6120 TABLET, FILM COATED in 1 BOTTLE (71335-3079-6)Feb 13, 2026
71335-3079-710 TABLET, FILM COATED in 1 BOTTLE (71335-3079-7)Feb 13, 2026
71335-3079-814 TABLET, FILM COATED in 1 BOTTLE (71335-3079-8)Feb 13, 2026
71335-3079-920 TABLET, FILM COATED in 1 BOTTLE (71335-3079-9)Feb 13, 2026

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