# Sevelamer Hydrochloride

NDC: 33342-241
Generic name: Sevelamer Hydrochloride
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230526

FDA application: ANDA206883

## Active ingredients

- SEVELAMER HYDROCHLORIDE: 400 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-241"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-241
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6926ebbe-2d74-4d5f-b642-c1bfe3a4e305
