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
- 16714-110_09ec5070-4e0b-4cf5-b3f1-67c0152b84a5
- Product NDC
- 16714-110
- Form
- TABLET, FILM COATED
- Composition / generic term
- Hydroxychloroquine sulfate
- Labeler
- Northstar Rx LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191001
- Source listing expiry
- 20261231
Source-listed ingredients
- HYDROXYCHLOROQUINE SULFATE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (16714-110-01) · 16714-110-01
- 500 TABLET, FILM COATED in 1 BOTTLE (16714-110-02) · 16714-110-02
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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