United States · FDA National Drug Code directory

HYDROXYCHLOROQUINE SULFATE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
55154-3567_ddab4d1a-867d-40df-8b31-fbbb9351b60b
Product NDC
55154-3567
Form
TABLET, FILM COATED
Composition / generic term
HYDROXYCHLOROQUINE SULFATE
Labeler
Cardinal Health 107, LLC
Marketing category
ANDA
Marketing start / end (source format)
20180501
Source listing expiry
20271231

Source-listed ingredients

  • HYDROXYCHLOROQUINE SULFATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 BLISTER PACK in 1 BAG (55154-3567-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 55154-3567-0

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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