# Maraviroc

NDC: 72319-024
Generic name: Maraviroc
Labeler / Manufacturer: i3 Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230915

FDA application: ANDA217114

## Active ingredients

- MARAVIROC: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72319-024"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72319-024
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f7b9c67b-10c6-45b5-b2a8-952cd350b0b1