# Mesalamine

NDC: 65162-360
Generic name: Mesalamine
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20250219

FDA application: ANDA215067

## Active ingredients

- MESALAMINE: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-360"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-360
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00f77203-3615-47e8-ae25-6e1cf8a2a00a