Structural Formula Dobutamine Hydrochloride (Image 01)
The text is not available.*
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.
Principal Display Panel (20 mL Vial Label)
This is a description of a medication called Dobutamine Injection, USP (250mg/20mL) contained in a 20mL single-dose vial. It is for intravenous use and must be diluted before usage. Each mL of the medication contains 12.5mg of dobutamine hydrochloride along with sodium metabisulfite and may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. The medication should be used within 24 hours after dilution and any unused portion should be discarded. The medication should be stored at room temperature, between 20° to 25°C (68° to 77°F). There is manufacturing information provided from Hainan Poly Pharm. Co., Ltd. in China. The expiration date is not available.*
Carton Label For 250 mg Per 20 mL (Image03)
Container Label For 500 mg Per 40 mL (Image04)
This is a prescription drug with the NDC code 14335-172-01. It is a single-dose vial containing 500mg/40ml (12.5mg/ml) of Dobutamine Injection, USP, used for intravenous administration. The drug must be diluted before use and should be used within 24 hours of dilution. Any unused portion should be discarded, and the drug must be stored at a temperature of 20° to 25°C (68° to 77°F). The drug contains sodium metabisulfite and may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. For more information on dilution, dosage, and administration, see the insert. The drug is manufactured by Hainan Poly Pharm. Co., Ltd. in Hainan Province, China 571127.*
Carton Label For 500 mg Per 40 mL (Image05)
This is a description of a medication called Dobutamine. It is an injection in a 40 ml single-dose vial, containing 500 mg/40 mL. It is for intravenous use only and must be diluted before use. Each ml contains 125 mg Dobutamine as the hydrochloride. The medication may also contain sodium chloride, hydrochloric acid, and/or sodium hydroxide to adjust the pH level. It is recommended to use the medication within 24 hours after dilution and to discard any unused portion. The medication needs to be stored between 20° to 25°C (68° to 77°F) or under controlled room temperature.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
