# QUININE SULFATE

NDC: 68180-560
Generic name: QUININE SULFATE
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20150804

FDA application: ANDA203112

## 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:"68180-560"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-560
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f32f05c-a215-40be-b951-e41a7b54a8a0