NDC 70710-2170 – Sevelamer carbonate

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

Human Prescription Drug

Product NDC70710-2170

Product details

Brand name
Sevelamer carbonate
Generic name
Sevelamer carbonate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA219931
Marketed since
April 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Phosphate Binder

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
70710-2170-330 TABLET, FILM COATED in 1 BOTTLE (70710-2170-3)Apr 1, 2026
70710-2170-7180 TABLET, FILM COATED in 1 BOTTLE (70710-2170-7)Apr 1, 2026
70710-2170-8270 TABLET, FILM COATED in 1 BOTTLE (70710-2170-8)Apr 1, 2026

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