NDC 70710-2058 – Sevelamer Hydrochloride

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

Human Prescription Drug

Product NDC70710-2058

Product details

Brand name
Sevelamer Hydrochloride
Generic name
Sevelamer Hydrochloride
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA218966
Marketed since
March 1, 2025
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
70710-2058-8180 TABLET, FILM COATED in 1 BOTTLE (70710-2058-8)Mar 1, 2025

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