Vfend Powder, For Suspension
Product Images NDC 0049-3160

Product Visual Gallery

This gallery contains 20 technical images submitted to the FDA as part of the official labeling for Vfend (NDC 0049-3160). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

FDA Label Image

Chemical Structure (Vfend 01)

Chemical structure of the active ingredient in VFEND, showing the molecular arrangement including fluorinated aromatic rings, a hydroxyl group, and a methyl substitution.*

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Logo (Vfend 02)

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Principal Display Panel (50 mg Tablet Bottle Label)

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Principal Display Panel (200 mg Tablet Bottle Label)

An instructional diagram showing components of the VFEND oral liquid medication dispenser system. Labeled parts include the Child-Resistant Bottle Cap, Bottle, Bottle Adapter, Plunger, Oral Dispenser, and Tip. The illustration clarifies how these parts fit together for medication administration.*

FDA Label Image

Principal Display Panel (200 mg Vial Label)

An instructional illustration showing a person using both hands to grip a bottle with a child-resistant cap. One hand is holding the bottle while the other is pushing down and turning the cap, demonstrating how to open it.*

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Principal Display Panel (200 mg Vial Carton)

An instructional illustration showing hands opening or closing a bottle by pressing down and turning the cap, indicated by downward arrows. The image is likely related to safe handling or administration instructions for VFEND, but contains no text or product details.*

FDA Label Image

Principal Display Panel (40 mg Bottle Label)

A grayscale image showing the top portion of a cylindrical bottle with an open threaded neck designed for a screw cap closure. The bottle is empty and has no visible label or markings. No other product-specific information is visible in the image.*

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Principal Display Panel (40 mg Bottle Carton)

An instructional illustration showing a hand holding a syringe while pushing the plunger downward. A dark arrow indicates the direction of movement for the plunger. The image likely demonstrates the correct technique for administering or preparing a dose using a syringe, relevant to VFEND products.*

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Vfend 09

An instructional illustration showing a hand using a syringe to draw liquid from a bottle. The syringe is inserted into the bottle through the cap, demonstrating a step of medication preparation or dosing.*

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Vfend 10

An instructional line drawing showing a hand holding a vial and a syringe. The syringe is being inserted into the vial, illustrating the process of drawing liquid medication from the vial into the syringe. No text or brand information is visible.*

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Vfend 11

An instructional diagram showing a person holding a vial upside down and withdrawing liquid into a syringe. The image demonstrates the proper technique to draw medication from a vial using a syringe with one hand stabilizing the vial and the other hand pulling the syringe plunger down.*

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Vfend 12

An instructional line drawing showing a hand holding a syringe that is being inserted into the stopper of a vial. The illustration likely represents medication preparation by drawing liquid from the vial into the syringe.*

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Vfend 13

An instructional illustration showing a person opening a screw-cap bottle by twisting the cap counterclockwise. The image depicts both hands holding and manipulating the bottle and cap, indicating the proper method to open the container.*

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Vfend 14

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Vfend 15

Label for Vfend (voriconazole) 50 mg tablets by Roerig, a division of Pfizer Inc. The label includes storage instructions (15°C to 30°C), dosage directions to see prescribing information, and states each tablet contains 50 mg voriconazole. The package contains 30 tablets and is marked Rx only. The product is made in Ireland.*

FDA Label Image

Vfend 16

VFEND 200 mg tablets label showing voriconazole as the active ingredient. The label indicates a package count of 30 tablets, distributed by Roerig, a division of Pfizer Inc. Storage instructions specify controlled room temperature between 15°C to 30°C. The label includes dosage guidance to refer to prescribing information.*

FDA Label Image

Vfend 17

VFEND I.V. 200 mg vial label for voriconazole injection by Roerig, a division of Pfizer. The label indicates the product strength as 200 mg of voriconazole per vial, for intravenous infusion only. It states the vial is sterile, single-dose with no preservatives and is not made with natural rubber latex. The label includes storage instructions and dispensing information.*

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Vfend 18

Packaging label for Vfend I.V. 200 mg (voriconazole) sterile single-dose vial for injection. The label states it is for intravenous infusion only, not made with natural rubber latex, and contains no preservatives. Distributed by Roerig, a division of Pfizer Inc. The label includes dosage preparation instructions and storage information.*

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Vfend 19

Label for Vfend oral suspension containing voriconazole 40 mg/mL, 75 mL bottle when reconstituted. The product is orange flavored and distributed by Roerig, a division of Pfizer Inc. Instructions specify refrigeration of dry powder before reconstitution and storage of suspension at controlled room temperature.*

FDA Label Image

Vfend 20

Packaging label for Vfend oral suspension 40 mg/mL (voriconazole), distributed by Roerig, division of Pfizer Inc. The label indicates an orange-flavored oral suspension with a 75 mL volume when reconstituted. It includes dosing instructions, storage conditions, and cautions such as shaking before use and discarding unused suspension after 14 days. The label features the Pfizer logo 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.