# Maraviroc

NDC: 68554-3079
Generic name: Maraviroc
Labeler / Manufacturer: Hetero Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220206

FDA application: ANDA203347

## 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:"68554-3079"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68554-3079
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9db91945-127e-4bb6-970a-ff1e36dde658