United States · FDA National Drug Code directory

SEVELAMER CARBONATE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
65862-931_e8c6db3c-3509-4033-8161-555236328bed
Product NDC
65862-931
Form
POWDER, FOR SUSPENSION
Composition / generic term
SEVELAMER CARBONATE
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20170613
Source listing expiry
20261231

Source-listed ingredients

  • SEVELAMER CARBONATE — 2400 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 POUCH in 1 CARTON (65862-931-90) / 1 POWDER, FOR SUSPENSION in 1 POUCH (65862-931-08) · 65862-931-90

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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