NDC 16714-632

Alendronate Sodium 35 mg tablet

On the label: Northstar Rx LLC..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aurobindo Pharma LimitedMedchal, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action

Product details

Generic drug
Alendronic Acid: every company that makes it
Form
tablet, oral
Strength
35 mg
Approval
ANDA ANDA090124
On the market since
Aug 4, 2008
Package NDCs
16714-632-01 16714-632-02 16714-632-10 16714-632-11
Official label
DailyMed (National Library of Medicine), updated Jun 12, 2026

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