NDC 0069-2250

Caduet 10 mg / 40 mg tablet, film coated

On the label: Pfizer Laboratories Div Pfizer Inc.

Ireland: 1Germany: 1United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Pfizer Ireland Pharmaceuticals Unlimited CompanyRingaskiddy, IrelandMakes the active ingredient and tests it Problems found, fixed voluntarilyOct 25, 2024 · 6 inspections
Pfizer Manufacturing Deutschland GmbHFreiburg im Breisgau, GermanyMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyJul 2, 2025 · 8 inspections
Viatris Pharmaceuticals LLCBarceloneta, PR, United StatesMakes the active ingredient No problems foundJun 13, 2025 · 8 inspections, 1 with FDA action
Pfizer IncChesterfield, MO, United StatesTests it No problems foundAug 20, 2019 · 4 inspections
Pharmacia & Upjohn Company LLCKalamazoo, MI, United StatesPackages it and labels it Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections
Viatris Pharmaceuticals LLCVega Baja, PR, United StatesPackages it Problems found, fixed voluntarilyMay 18, 2026 · 11 inspections

Recalls

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

Product details

Generic drug
Amlodipine and Atorvastatin: every company that makes it
Form
tablet, film coated
Strength
10 mg / 40 mg
Approval
NDA NDA021540
On the market since
Jan 30, 2004
Package NDCs
0069-2250-30
Official label
DailyMed (National Library of Medicine), updated Jun 25, 2026

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