# ALLI

NDC: 0135-0461
Generic name: orlistat
Labeler / Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20070207

FDA application: NDA021887

## Active ingredients

- ORLISTAT: 60 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0135-0461"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0135-0461
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a2d3bd73-f3af-4ea5-a57c-66b0004cfe4f