# PRIMAQUINE PHOSPHATE

NDC: 50742-191
Generic name: PRIMAQUINE PHOSPHATE
Labeler / Manufacturer: Ingenus Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180123

FDA application: ANDA206043

## Active ingredients

- PRIMAQUINE PHOSPHATE: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50742-191"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50742-191
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=09531382-2e06-4164-a7e1-169a1488788a