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
- 0904-7046_32eabaf6-e837-4b40-bee2-dbeea2238e2c
- Product NDC
- 0904-7046
- Form
- TABLET, FILM COATED
- Composition / generic term
- HYDROXYCHLOROQUINE SULFATE
- Labeler
- Major Pharmaceuticals
- 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
- 50 BLISTER PACK in 1 CARTON (0904-7046-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 0904-7046-06
- 100 BLISTER PACK in 1 CARTON (0904-7046-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK · 0904-7046-61
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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