NDC 72162-2501 – Sevelamer Hydrochloride

Sevelamer Hydrochloride 800 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-2501

Product details

Brand name
Sevelamer Hydrochloride
Generic name
Sevelamer Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206883
Marketed since
May 26, 2023
Listing expires
December 31, 2026
Pharmacologic class
Phosphate Binder

Active ingredients

Uses, dosage, side effects and warnings for Sevelamer Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
72162-2501-2180 TABLET, FILM COATED in 1 BOTTLE (72162-2501-2)May 15, 2025

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