# VIVITROL

NDC: 65757-301
Generic name: naltrexone
Labeler / Manufacturer: Alkermes, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: KIT
Routes: —
Marketing started: 20060613

FDA application: NDA021897

## Active ingredients

—

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65757-301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65757-301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cd11c435-b0f0-4bb9-ae78-60f101f3703f