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
- 68382-824_c36f7488-a329-4113-8027-dfc92bbc6bbc
- Product NDC
- 68382-824
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sevelamer carbonate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200917
- Source listing expiry
- 20261231
Source-listed ingredients
- SEVELAMER CARBONATE — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (68382-824-10) · 68382-824-10
- 270 TABLET, FILM COATED in 1 BOTTLE (68382-824-27) · 68382-824-27
- 10 BLISTER PACK in 1 CARTON (68382-824-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-824-30) · 68382-824-77
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 →