NDC 76420-850 – Hydroxychloroquine sulfate

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

Human Prescription Drug

Product NDC76420-850

Product details

Brand name
Hydroxychloroquine sulfate
Generic name
Hydroxychloroquine sulfate
Labeler
Asclemed USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040657
Marketed since
October 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
76420-850-01100 TABLET, FILM COATED in 1 BOTTLE (76420-850-01)Sep 5, 2024
76420-850-05500 TABLET, FILM COATED in 1 BOTTLE (76420-850-05)Sep 5, 2024
76420-850-3030 TABLET, FILM COATED in 1 BOTTLE (76420-850-30)Sep 5, 2024
76420-850-6060 TABLET, FILM COATED in 1 BOTTLE (76420-850-60)Sep 5, 2024
76420-850-9090 TABLET, FILM COATED in 1 BOTTLE (76420-850-90)Sep 5, 2024

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