NDC 69097-223

Alendronate Sodium 35 mg tablet

On the label: Cipla USA., Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Cipla LimitedSalcette, IndiaMakes it Problems found, fixed voluntarilyJun 21, 2024 · 12 inspections, 2 with FDA action

Product details

Generic drug
Alendronic Acid: every company that makes it
Form
tablet, oral
Strength
35 mg
Approval
ANDA ANDA076768
On the market since
Aug 4, 2008
Package NDCs
69097-223-16 69097-223-76
Official label
DailyMed (National Library of Medicine), updated Mar 25, 2026

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