Caduet
Product Images NDC 0069-2150

25 FDA label images from Pfizer Laboratories Div Pfizer Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 25 technical images submitted to the FDA as part of the official labeling for Caduet (NDC 0069-2150). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pfizer Laboratories Div Pfizer Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Chemical Structure (Caduet 01)

Chemical Structure (Caduet 01)
Chemical structure of the active ingredient in Caduet, showing a complex molecule with chlorine, oxygen, nitrogen, carbon, and hydrogen atoms, including functional groups such as amine, ester, and ether moieties.*
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Chemical Structure (Caduet 02)

Chemical Structure (Caduet 02)
Chemical structure diagram of the active ingredient in Caduet, showing molecular bonds and the associated calcium and water molecules as part of the compound's complex form.*
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Figure 1 (Caduet 03)

Figure 1 (Caduet 03)
A line graph comparing event rates over time (in months) between two groups labeled Placebo and Amlodipine. The x-axis shows time up to 24 months, and the y-axis shows event rate from 0 to 0.25. The graph includes a statistical box with P-value=0.003, Hazard Ratio=0.691, and 95% Confidence Interval=0.54 to 0.88. Numbers at risk are noted along the time axis for both groups.*
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Figure 2 (Caduet 04)

Figure 2 (Caduet 04)
A forest plot displaying hazard ratios with 95% confidence intervals comparing the effect of Amlodipine versus Placebo across various patient subgroups, including age, gender, baseline sitting systolic blood pressure, baseline vessel disease, baseline vessels with stenosis, and PCI-stent strata. The horizontal axis shows hazard ratio values ranging from 0.0 to 2.0, with markers indicating the estimated hazard ratios for each subgroup relative to Amlodipine favoring or placebo favoring outcomes.*
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Figure 3 (Caduet 05)

Figure 3 (Caduet 05)
A line graph showing cumulative incidence percentage over time in years (0 to 3.5) comparing Atorvastatin and placebo. The solid line represents Atorvastatin and the dashed line represents placebo, with placebo showing higher cumulative incidence across the period. Additional text shows hazard ratio (HR=0.64) with confidence intervals and a p-value.*
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Figure 4 (Caduet 06)

Figure 4 (Caduet 06)
A Kaplan-Meier cumulative hazard graph showing the percentage of events over time from 0 to 5 years. It compares two groups, Placebo (dashed line) and Atorvastatin (solid line), with Atorvastatin showing a lower cumulative hazard percentage over the follow-up period. The graph includes a hazard ratio (HR 0.63, 95% CI 0.48-0.83) and a p-value of 0.001 indicating statistical analysis results.*
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Figure 5 (Caduet 07)

Figure 5 (Caduet 07)
A line graph comparing the percentage of subjects experiencing a major cardiovascular event over five years for Atorvastatin 10 mg and Atorvastatin 80 mg. The x-axis represents time to first major cardiovascular endpoint in years, and the y-axis shows the percentage of subjects experiencing the event. Atorvastatin 80 mg shows a lower event rate, with hazard ratio 0.78 (0.69-0.89), P=0.0002.*
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Logo (Caduet 08)

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Logo (Caduet 09)

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Principal Display Panel (2.5 mg/10 mg Tablet Bottle Label)

Principal Display Panel (2.5 mg/10 mg Tablet Bottle Label)
Caduet 5 mg/10 mg tablets label showing the active ingredients amlodipine besylate and atorvastatin calcium. The label includes storage instructions at 25°C (77°F) with excursions permitted to 15-30°C, distributor information for Pfizer Labs, and indicates a 30-tablet count. The label features the Pfizer logo and is marked Rx only.*
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Principal Display Panel (2.5 mg/20 mg Tablet Bottle Label)

Principal Display Panel (2.5 mg/20 mg Tablet Bottle Label)
Caduet 5 mg/20 mg tablets label showing active ingredients amlodipine besylate and atorvastatin calcium. The label includes storage instructions, dosing information, and manufacturer details Pfizer Labs, Division of Pfizer Inc. The package contains 30 tablets and is marked Rx only. NDC 0069-2170-30 is visible alongside a barcode.*
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Principal Display Panel (2.5 mg/40 mg Tablet Bottle Label)

Principal Display Panel (2.5 mg/40 mg Tablet Bottle Label)
Caduet 5 mg/40 mg tablets label shows the active ingredients amlodipine besylate and atorvastatin calcium. The label includes storage instructions, dosage and use notes, and manufacturer Pfizer Laboratories Division of Pfizer Inc. The package contains 30 tablets and is marked Rx only. Barcode and lot/expiration placeholders are visible.*
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Principal Display Panel (5 mg/10 mg Tablet Bottle Label)

Principal Display Panel (5 mg/10 mg Tablet Bottle Label)
Label for Caduet tablets containing 5 mg amlodipine besylate and 80 mg atorvastatin calcium, distributed by Pfizer Labs, Division of Pfizer Inc, NY. The label indicates 30 tablets per package, storage instructions, and product identification codes including NDC 0069-2260-30 and GTIN 00300692260301.*
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Principal Display Panel (5 mg/20 mg Tablet Bottle Label)

Principal Display Panel (5 mg/20 mg Tablet Bottle Label)
Label for Caduet tablets containing 10 mg amlodipine besylate and 10 mg atorvastatin calcium. The label shows the Pfizer logo and indicates the product is supplied by Pfizer Labs, made in Germany. It includes storage instructions, a barcode, and states the package contains 30 tablets, Rx only.*
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Principal Display Panel (5 mg/40 mg Tablet Bottle Label)

Principal Display Panel (5 mg/40 mg Tablet Bottle Label)
Label for Caduet tablets containing amlodipine besylate and atorvastatin calcium, strength 10 mg/20 mg. The label shows the Pfizer logo and indicates a package of 30 tablets, prescription only. Storage instructions and distributor information (Pfizer Labs, NY) are also visible.*
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Principal Display Panel (5 mg/80 mg Tablet Bottle Label)

Principal Display Panel (5 mg/80 mg Tablet Bottle Label)
Label for Caduet tablets by Pfizer Laboratories, showing active ingredients amlodipine besylate and atorvastatin calcium in strength 10 mg/40 mg. The label includes storage instructions, distributor information, package count of 30 tablets, Rx only status, and a barcode with NDC 0069-2250-30. Manufactured in Germany.*
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Principal Display Panel (10 mg/10 mg Tablet Bottle Label)

Principal Display Panel (10 mg/10 mg Tablet Bottle Label)
Caduet tablets label showing amlodipine besylate 10 mg and atorvastatin calcium 80 mg strength. The label includes the Pfizer logo, NDC 0069-2270-30, and indicates a 30-tablet count. The product is distributed by Pfizer Labs Division of Pfizer Inc, made in Germany, and marked Rx only.*
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Principal Display Panel (10 mg/20 mg Tablet Bottle Label)

Principal Display Panel (10 mg/20 mg Tablet Bottle Label)
Label for Caduet tablets containing 5 mg amlodipine and 10 mg atorvastatin. The label includes storage instructions, dosage and use note, distributed by Pfizer Labs, division of Pfizer Inc, made in Germany. The package contains 30 tablets and states Rx only. Barcode and NDC 0069-6180-30 are visible.*
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Principal Display Panel (10 mg/40 mg Tablet Bottle Label)

Principal Display Panel (10 mg/40 mg Tablet Bottle Label)
Caduet 5 mg/20 mg tablets label showing active ingredients amlodipine and atorvastatin. The label includes the Pfizer logo, NDC 0069-6323-30, 30 tablets per package, and indicates prescription use only. It states storage conditions, manufacturing in Germany, and distribution by Pfizer Labs, Division of Pfizer Inc.*
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Principal Display Panel (10 mg/80 mg Tablet Bottle Label)

Principal Display Panel (10 mg/80 mg Tablet Bottle Label)
Label for Caduet tablets containing amlodipine and atorvastatin, strength 5 mg/40 mg. The label includes Pfizer's logo, NDC 0069-6565-30, and states a package size of 30 tablets. It highlights storage temperature instructions, dosage and use directions referencing accompanying prescribing information, and manufacturing details indicating distribution by Pfizer Labs, made in Germany. Barcode and GTIN information are also visible.*
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Caduet 21

Caduet 21
Caduet 5 mg/80 mg tablets label shows the active ingredients amlodipine and atorvastatin. The label indicates the package contains 30 tablets and is distributed by Pfizer Labs, Division of Pfizer Inc, New York, NY. Additional storage information and warnings are included, noting the product is for prescription use only.*
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Caduet 22

Caduet 22
Label for Caduet 10 mg/10 mg tablets containing amlodipine and atorvastatin. The label indicates a package size of 30 tablets, distributed by Pfizer Laboratories Division of Pfizer Inc. Storage instructions specify 25°C with allowable excursions. The label includes dosage information referencing accompanying prescribing information and states the product is Rx only.*
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Caduet 23

Caduet 23
Label for Caduet tablets containing amlodipine and atorvastatin, strength 10 mg/20 mg. The label shows Pfizer as the labeler, NDC 0069-7232-30, with a 30-tablet count, and storage instructions. It includes dosage and use notes, barcodes, and batch information sections.*
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Caduet 24

Caduet 24
Label for Caduet tablets containing 10 mg amlodipine and 40 mg atorvastatin. The label includes storage instructions, dosage and use notes, distributor information (Pfizer Labs Division, Pfizer Inc), and package count of 30 tablets. It features the Pfizer logo, NDC code 0069-7654-30, and a barcode.*
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Caduet 25

Caduet 25
Label for Caduet tablets containing 10 mg amlodipine and 80 mg atorvastatin. The label indicates a package of 30 tablets, Rx only, distributed by Pfizer Labs, Division of Pfizer Inc, NY. Storage instructions specify 25°C with permitted excursions. The label includes NDC 0069-7476-30 and a barcode.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.