NDC 42385-971 – Hydroxychloroquine Sulfate

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

Human Prescription Drug

Product NDC42385-971

Product details

Brand name
Hydroxychloroquine Sulfate
Generic name
Hydroxychloroquine Sulfate
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210959
Marketed since
March 6, 2023
Listing expires
December 31, 2026
Pharmacologic class
Antimalarial; Antirheumatic Agent

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
42385-971-01100 TABLET, FILM COATED in 1 BOTTLE (42385-971-01)Mar 6, 2023
42385-971-05500 TABLET, FILM COATED in 1 BOTTLE (42385-971-05)Mar 6, 2023
42385-971-111000 TABLET, FILM COATED in 1 BOTTLE (42385-971-11)Mar 6, 2023
42385-971-6060 TABLET, FILM COATED in 1 BOTTLE (42385-971-60)Mar 6, 2023

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