United States · FDA National Drug Code directory
QUININE 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
- 50742-238_0a0b38d3-828f-4828-8d8c-92933872aa4f
- Product NDC
- 50742-238
- Form
- CAPSULE
- Composition / generic term
- QUININE SULFATE
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171211
- Source listing expiry
- 20261231
Source-listed ingredients
- QUININE SULFATE — 324 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE, PLASTIC (50742-238-30) · 50742-238-30
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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