NDC 71335-1771 – Hydroxychloroquine Sulfate

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

Human Prescription Drug

Product NDC71335-1771

Product details

Brand name
Hydroxychloroquine Sulfate
Generic name
Hydroxychloroquine Sulfate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040081
Marketed since
October 8, 2020
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
71335-1771-1100 TABLET, FILM COATED in 1 BOTTLE (71335-1771-1)Sep 2, 2021
71335-1771-230 TABLET, FILM COATED in 1 BOTTLE (71335-1771-2)Aug 19, 2021
71335-1771-360 TABLET, FILM COATED in 1 BOTTLE (71335-1771-3)Dec 29, 2021
71335-1771-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1771-4)Jan 21, 2021
71335-1771-590 TABLET, FILM COATED in 1 BOTTLE (71335-1771-5)Dec 29, 2021
71335-1771-6120 TABLET, FILM COATED in 1 BOTTLE (71335-1771-6)Dec 29, 2021
71335-1771-710 TABLET, FILM COATED in 1 BOTTLE (71335-1771-7)Aug 16, 2021
71335-1771-814 TABLET, FILM COATED in 1 BOTTLE (71335-1771-8)Dec 29, 2021
71335-1771-920 TABLET, FILM COATED in 1 BOTTLE (71335-1771-9)Aug 18, 2021

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