NDC 0069-2180

Caduet 10 mg / 20 mg tablet, film coated

Where it's made

Factory	Where	Role	Last FDA inspection
Pfizer Ireland Pharmaceuticals Unlimited Company	Ringaskiddy, Ireland	Makes the active ingredient and tests it	Problems found, fixed voluntarilyOct 25, 2024 · 6 inspections
Pfizer Manufacturing Deutschland GmbH	Freiburg im Breisgau, Germany	Makes it, tests it, packages it and labels it	Problems found, fixed voluntarilyJul 2, 2025 · 8 inspections
Viatris Pharmaceuticals LLC	Barceloneta, PR, United States	Makes the active ingredient	No problems foundJun 13, 2025 · 8 inspections, 1 with FDA action
Pfizer Inc	Chesterfield, MO, United States	Tests it	No problems foundAug 20, 2019 · 4 inspections
Pharmacia & Upjohn Company LLC	Kalamazoo, MI, United States	Packages it and labels it	Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections
Viatris Pharmaceuticals LLC	Vega Baja, PR, United States	Packages it	Problems found, fixed voluntarilyMay 18, 2026 · 11 inspections

Feb 5, 2020 · Class II · Pfizer Inc.
Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture protection.
Lots: Lot #: CY0937, Exp 12/2021
Feb 5, 2020 · Class II · Pfizer Inc.
Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture protection.
Lots: Lot #: CY0963, Exp 07/2022

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Generic drug: Amlodipine and Atorvastatin: every company that makes it
Form: tablet, film coated
Strength: 10 mg / 20 mg
Approval: NDA NDA021540
On the market since: Jan 30, 2004
Package NDCs: 0069-2180-30
Official label: DailyMed (National Library of Medicine), updated Jun 25, 2026

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