Verapamil Hydrochloride
Product Images NDC 0409-9633

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Verapamil Hydrochloride (NDC 0409-9633). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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.

FDA Label Image

Structural Formula Verapamil Hydrochloride (Verapamil 01)

Chemical structure of verapamil hydrochloride, showing the molecular arrangement of atoms including aromatic rings, methoxy groups, a nitrile group, and a hydrochloride component.*

FDA Label Image

Logo (Verapamil 02)

FDA Label Image

Principal Display Panel (4 mL Vial Label)

Label for Verapamil Hydrochloride Injection, USP, 10 mg per 4 mL (2.5 mg/mL) single-dose vial. Indicated for intravenous use only, with instructions to protect from light. Distributed by Hospira, Inc., Lake Forest, IL. NDC 0409-1144-62 and barcode present.*

FDA Label Image

Principal Display Panel (4 mL Vial Carton)

Packaging label for Verapamil Hydrochloride Injection, USP, 10 mg/4 mL (2.5 mg/mL) in a 4 mL single-dose fliptop vial. The label shows storage instructions, NDC numbers 0409-1144-02 and 0409-1144-62, and indicates the product is manufactured in Italy and distributed by Hospira, Inc. Contains bar code and additional drug ingredient details on the label.*

FDA Label Image

Principal Display Panel (2 mL Vial Label)

Label for Verapamil Hydrochloride Injection USP, 5 mg/2 mL concentration (2.5 mg/mL strength), presented as a 2 mL single-dose vial. The product is for intravenous use only and distributed by Hospira, Inc., Lake Forest, IL. The label includes storage instructions to protect from light and shows the NDC 0409-1144-65 along with a barcode and space for lot and expiration details.*

FDA Label Image

Principal Display Panel (2 mL Vial Carton)

Packaging label for Verapamil Hydrochloride Injection, USP 5 mg/2 mL (2.5 mg/mL) single-dose fliptop vials. Contains 25 vials of 2 mL each. The product is for intravenous use only and labeled Rx only. Manufactured by Hospira, Inc., distributed from Lake Forest, IL, USA, and made in Italy. Storage instructions note protecting from light and storing at 20 to 25°C (68 to 77°F).*

FDA Label Image

Principal Display Panel (2 mL Ampul Label)

Verapamil Hydrochloride Injection, USP label displaying 5 mg per 2 mL (2.5 mg/mL) strength. The label indicates it is for intravenous use only, and includes storage instructions to protect from light. Distributed by Hospira, Inc., Lake Forest, IL. The label also shows an NDC number and a barcode.*

FDA Label Image

Principal Display Panel (2 mL Ampul Container Label)

Label for Verapamil Hydrochloride Injection, USP 5 mg/2 mL (2.5 mg/mL) single-dose ampuls. The label indicates five ampuls per package, for intravenous use only, provided by Hospira, Inc. The label includes storage instructions, ingredient details, and is marked for Rx only. It is made in Italy and distributed by Hospira, Inc.*

FDA Label Image

Principal Display Panel (4 mL Syringe Label)

Label for Verapamil HCl Injection, USP, 10 mg/4 mL (2.5 mg/mL) in a single-dose 4 mL syringe, distributed by Hospira, Inc. The label indicates the product is for intravenous use only, requires protection from light, and is Rx only. The NDC is 0409-9633-65.*

FDA Label Image

Principal Display Panel (4 mL Syringe Carton)

Packaging label for Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL) in a 4 mL single-dose syringe by Hospira, Inc. The label includes usage instructions for aseptic technique, storage instructions to protect from light, and specifies intravenous use only. It also notes the product is made in Italy and distributed by Hospira, Inc.*

* 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.