# QUININE SULFATE

NDC: 50742-238
Generic name: QUININE SULFATE
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20171211

FDA application: ANDA204372

## Active ingredients

- QUININE SULFATE: 324 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-238"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-238
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2f73c64-b92c-49bf-ad39-e32ac83e4d3d