# MESALAMINE

NDC: 0527-3012
Generic name: mesalamine
Labeler / Manufacturer: Lannett Company Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20230603

FDA application: ANDA217337

## 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:"0527-3012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-3012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=29dbe417-15a9-4c4d-846b-81cabda7ac70