# SEVELAMER CARBONATE

NDC: 65862-930
Generic name: SEVELAMER CARBONATE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20170613

FDA application: ANDA207624

## 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:"65862-930"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-930
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ea201bff-cdfb-4304-bdb1-d05c1dac2677