NDC 62135-752 – Hydroxychloroquine

Hydroxychloroquine Sulfate 200 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62135-752

Product details

Brand name
Hydroxychloroquine
Generic name
Hydroxychloroquine
Labeler
Chartwell RX, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210543
Marketed since
July 6, 2018
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

Uses, dosage, side effects and warnings for Hydroxychloroquine →

Package NDC codes (1)

Package NDCDescriptionSince
62135-752-9090 TABLET in 1 BOTTLE (62135-752-90)May 28, 2024