NDC 57664-761 – Hydroxychloroquine sulfate

Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC57664-761

Product details

Brand name
Hydroxychloroquine sulfate
Generic name
Hydroxychloroquine sulfate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201691
Marketed since
June 18, 2018
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
57664-761-13500 TABLET in 1 BOTTLE (57664-761-13)Jun 18, 2018
57664-761-88100 TABLET in 1 BOTTLE (57664-761-88)Jun 18, 2018

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