NDC 71335-0897 – Hydroxychloroquine sulfate

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

Human Prescription Drug

Product NDC71335-0897

Product details

Brand name
Hydroxychloroquine sulfate
Generic name
Hydroxychloroquine sulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040657
Marketed since
January 3, 2008
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-0897-1100 TABLET, FILM COATED in 1 BOTTLE (71335-0897-1)Jul 14, 2020
71335-0897-230 TABLET, FILM COATED in 1 BOTTLE (71335-0897-2)Mar 13, 2020
71335-0897-360 TABLET, FILM COATED in 1 BOTTLE (71335-0897-3)Jul 6, 2018
71335-0897-4180 TABLET, FILM COATED in 1 BOTTLE (71335-0897-4)Jul 10, 2018
71335-0897-590 TABLET, FILM COATED in 1 BOTTLE (71335-0897-5)Feb 25, 2019
71335-0897-6120 TABLET, FILM COATED in 1 BOTTLE (71335-0897-6)Jul 9, 2024
71335-0897-710 TABLET, FILM COATED in 1 BOTTLE (71335-0897-7)Jul 9, 2024
71335-0897-814 TABLET, FILM COATED in 1 BOTTLE (71335-0897-8)Jul 9, 2024
71335-0897-920 TABLET, FILM COATED in 1 BOTTLE (71335-0897-9)Jul 9, 2024

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