# SEVELAMER CARBONATE

NDC: 58624-5001
Generic name: SEVELAMER CARBONATE
Labeler / Manufacturer: Shandong Xinhua Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250227

FDA application: ANDA215998

## Active ingredients

- SEVELAMER CARBONATE: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"58624-5001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58624-5001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6455fa3-ad53-f6fd-e053-2a95a90a67db