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
- 65162-058_53f81fb7-7bbc-430f-a2e4-841b58e2cb7c
- Product NDC
- 65162-058
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sevelamer Carbonate
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171128
- Source listing expiry
- 20261231
Source-listed ingredients
- SEVELAMER CARBONATE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (65162-058-03) · 65162-058-03
- 60 TABLET, FILM COATED in 1 BOTTLE (65162-058-06) · 65162-058-06
- 90 TABLET, FILM COATED in 1 BOTTLE (65162-058-09) · 65162-058-09
- 1000 TABLET, FILM COATED in 1 BOTTLE (65162-058-11) · 65162-058-11
- 270 TABLET, FILM COATED in 1 BOTTLE (65162-058-27) · 65162-058-27
- 500 TABLET, FILM COATED in 1 BOTTLE (65162-058-50) · 65162-058-50
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →