# Sevelamer Carbonate

NDC: 17856-0921
Generic name: Sevelamer Carbonate
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180627

FDA application: ANDA207179

## 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:"17856-0921"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0921
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07b709fd-a2a1-4ff1-ad19-827d38e84562