NDC 54868-5209
Caduet 10 mg / 20 mg tablet, film coated
On the label: Physicians Total Care, Inc.. It's repackaged: Physicians Total Care, Inc. rebottles it from Pfizer Laboratories Div Pfizer Inc's NDC 0069-2180.
Where the pills inside were 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 |
Recalls
- 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.
Product details
- 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 18, 2005
- Package NDCs
54868-5209-054868-5209-1- Official label
- DailyMed (National Library of Medicine), updated Nov 30, 2009
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