NDC 69584-022

AMLODIPINE BESYLATE5 mg 5 mg tablet

On the label: Oxford Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Oxford Pharmaceuticals, LLCBirmingham, AL, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections

Product details

Generic drug
Amlodipine: every company that makes it
Form
tablet, oral
Strength
5 mg
Approval
ANDA ANDA078414
On the market since
Oct 1, 2021
Package NDCs
69584-022-09 69584-022-50 69584-022-90 69584-022-95
Official label
DailyMed (National Library of Medicine), updated Mar 28, 2026

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