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
- 55111-789_f4b7a1eb-7592-27f3-1316-50b7d2538cd1
- Product NDC
- 55111-789
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sevelamer Carbonate
- Labeler
- DR. REDDY'S LABORATORIES LIMITED
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170929
- Source listing expiry
- 20261231
Source-listed ingredients
- SEVELAMER CARBONATE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 25 BLISTER PACK in 1 CARTON (55111-789-11) / 4 TABLET, FILM COATED in 1 BLISTER PACK (55111-789-48) · 55111-789-11
- 270 TABLET, FILM COATED in 1 BOTTLE (55111-789-27) · 55111-789-27
- 30 TABLET, FILM COATED in 1 BOTTLE (55111-789-30) · 55111-789-30
- 90 TABLET, FILM COATED in 1 BOTTLE (55111-789-90) · 55111-789-90
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 →