# Maraviroc

NDC: 68475-008
Generic name: Maraviroc
Labeler / Manufacturer: Navinta LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250623

FDA application: ANDA217880

## 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:"68475-008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68475-008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=211290a4-5e26-4784-aa99-8ccaf2eaaa15