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
- 72162-2499_3bc019bd-1222-418b-aa92-da358c0dc2fa
- Product NDC
- 72162-2499
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sevelamer Carbonate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230419
- Source listing expiry
- 20271231
Source-listed ingredients
- SEVELAMER CARBONATE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (72162-2499-1) · 72162-2499-1
- 270 TABLET, FILM COATED in 1 BOTTLE (72162-2499-2) · 72162-2499-2
- 50 TABLET, FILM COATED in 1 BOTTLE (72162-2499-4) · 72162-2499-4
- 90 TABLET, FILM COATED in 1 BOTTLE (72162-2499-9) · 72162-2499-9
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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