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: 71610-961_427ac308-f737-d1f0-e063-6294a90ae7a0
Product NDC: 71610-961
Form: TABLET, FILM COATED
Composition / generic term: Hydroxychloroquine Sulfate
Labeler: Aphena Pharma Solutions - Tennessee, LLC
Marketing category: ANDA
Marketing start / end (source format): 20180517
Source listing expiry: 20261231

Source-listed ingredients

HYDROXYCHLOROQUINE SULFATE — 200 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, FILM COATED in 1 BOTTLE (71610-961-30) · 71610-961-30
60 TABLET, FILM COATED in 1 BOTTLE (71610-961-53) · 71610-961-53
180 TABLET, FILM COATED in 1 BOTTLE (71610-961-80) · 71610-961-80

Source and coverage

Open FDA National Drug Code directory →

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.

Browse United States records →