NDC 16571-112 – Hydroxychloroquine Sulfate

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

Human Prescription Drug

Product NDC16571-112

Product details

Brand name
Hydroxychloroquine Sulfate
Generic name
Hydroxychloroquine Sulfate
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA210959
Marketed since
May 29, 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
16571-112-01100 TABLET, FILM COATED in 1 BOTTLE (16571-112-01)May 29, 2023
16571-112-0660 TABLET, FILM COATED in 1 BOTTLE (16571-112-06)May 29, 2023
16571-112-101000 TABLET, FILM COATED in 1 BOTTLE (16571-112-10)May 29, 2023
16571-112-50500 TABLET, FILM COATED in 1 BOTTLE (16571-112-50)May 29, 2023

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