NDC 70748-173 – Sevelamer hydrochloride

Sevelamer Hydrochloride 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70748-173

Product details

Brand name
Sevelamer hydrochloride
Generic name
Sevelamer hydrochloride
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213145
Marketed since
February 25, 2022
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
70748-173-26180 TABLET in 1 BOTTLE (70748-173-26)Feb 25, 2022

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