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
- 58624-5001_ff5f602e-c050-40d7-81f5-1c8dfba1d32f
- Product NDC
- 58624-5001
- Form
- TABLET, FILM COATED
- Composition / generic term
- SEVELAMER CARBONATE
- Labeler
- Shandong Xinhua Pharmaceutical Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250227
- 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 (58624-5001-2) · 58624-5001-2
- 18399 TABLET, FILM COATED in 1 CARTON (58624-5001-4) · 58624-5001-4
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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