# Mesalamine

NDC: 84612-175
Generic name: Mesalamine
Labeler / Manufacturer: Nuvaila Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20260701

FDA application: ANDA211858

## Active ingredients

- MESALAMINE: 1.2 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"84612-175"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=84612-175
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=875d573f-99a1-426a-8321-4d511690d503