NDC 70748-173

Sevelamer hydrochloride 800 mg tablet

On the label: Lupin Pharmaceuticals, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Lupin LimitedNagpur, IndiaMakes it and packages it Problems found, fixed voluntarilyJul 11, 2023 · 4 inspections

Product details

Generic drug
Sevelamer: every company that makes it
Form
tablet, oral
Strength
800 mg
Approval
ANDA ANDA213145
On the market since
Feb 25, 2022
Package NDCs
70748-173-26
Official label
DailyMed (National Library of Medicine), updated Jul 22, 2025

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