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
- 65862-921_761597e6-1a2e-48e7-b657-c3fa781b4f6b
- Product NDC
- 65862-921
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sevelamer Carbonate
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170717
- Source listing expiry
- 20261231
Source-listed ingredients
- SEVELAMER CARBONATE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 180 TABLET, FILM COATED in 1 BOTTLE (65862-921-18) · 65862-921-18
- 270 TABLET, FILM COATED in 1 BOTTLE (65862-921-27) · 65862-921-27
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-921-30) · 65862-921-30
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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