Dobutamine
Product Images NDC 14335-172

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dobutamine (NDC 14335-172). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hainan Poly Pharm. Co., Ltd., 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 Dobutamine Hydrochloride (Image 01)

Structural Formula Dobutamine Hydrochloride (Image 01)
Chemical structure of Dobutamine hydrochloride showing its key functional groups including hydroxyl and amine groups on aromatic rings and side chains.*
FDA Label Image

Principal Display Panel (20 mL Vial Label)

Principal Display Panel (20 mL Vial Label)
Label for Dobutamine Injection, USP 250 mg/20 mL (12.5 mg/mL) single-dose vial. The label states intravenous use only and requires dilution prior to use. It includes manufacturer details: Hainan Poly Pharm. Co., Ltd., Hainan Province, China. Storage instructions and additional product information are also given, along with a barcode and a logo for the manufacturer.*
FDA Label Image

Carton Label For 250 mg Per 20 mL (Image03)

Carton Label For 250 mg Per 20 mL (Image03)
Packaging label for Dobutamine Injection, USP 250 mg/20 mL (12.5 mg/mL) sterile single-dose vial by Hainan Poly Pharm. Co., Ltd. The label highlights that it is for intravenous use only and must be diluted prior to use. Storage instructions specify 20° to 25°C. The label includes barcode and regulatory info with lot and expiration date areas.*
FDA Label Image

Container Label For 500 mg Per 40 mL (Image04)

Container Label For 500 mg Per 40 mL (Image04)
Dobutamine Injection, USP 500 mg/40 mL (12.5 mg/mL) in a 40 mL single-dose vial by Hainan Poly Pharm. Co., Ltd. The label includes dosing information, storage conditions, and a barcode. It highlights that the product is for intravenous use only and must be diluted prior to use. Lot and expiration date areas are provided but not filled in.*
FDA Label Image

Carton Label For 500 mg Per 40 mL (Image05)

Carton Label For 500 mg Per 40 mL (Image05)
Dobutamine Injection, USP 500 mg/40 mL (12.5 mg/mL) packaging label for a 40 mL single-dose vial. The label indicates the product is for intravenous use only and must be diluted prior to use. Manufactured by Hainan Poly Pharm. Co., Ltd. The label includes handling and storage instructions and a barcode with the NDC 14335-1720-1.*

* 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.