United States · FDA National Drug Code directory
sevelamer hydrochloride
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
- 68462-446_5b27539f-4664-4a6b-abe4-2abcc7ad2279
- Product NDC
- 68462-446
- Form
- TABLET, FILM COATED
- Composition / generic term
- sevelamer hydrochloride
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190208
- Source listing expiry
- 20271231
Source-listed ingredients
- SEVELAMER HYDROCHLORIDE — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 360 TABLET, FILM COATED in 1 BOTTLE (68462-446-26) · 68462-446-26
- 30 TABLET, FILM COATED in 1 BOTTLE (68462-446-30) · 68462-446-30
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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