Dopamine Hydrochloride In Dextrose Injection, Solution
Product Images NDC 0409-0042

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Dopamine Hydrochloride In Dextrose (NDC 0409-0042). 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.

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Chemical Structure (Dopamine 01)

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Chemical Structure (Dopamine 02)

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Logo (Dopamine 03)

FDA Label Image

Principal Display Panel (250 mL Bag Label)

This is a description of a medication called DOPamine HCI (in 5% Dextrose Injection, USP), which is a single dose container that contains 400 mg/250 mL. The medication contains hydrochlorides and other chemicals to regulate pH levels, and it needs to be visually inspected before use to ensure it is not damaged or discolored in any way, which can affect its sterility. The medication must be stored at a controlled room temperature to prevent spoilage. The text also contains instructions on how to open and use the medication safely, as well as a warning about sulfites. However, it is not clear for what condition or disease the medication is intended.*

FDA Label Image

Principal Display Panel (250 mL Bag Label)

This is a description of a medication called Dopamine HCI that comes in 250mL of 5% Dextrose Injection, USP. The pack contains 300mg/250mL of the Dopamine HCI medication. Each 100mL of the content of the container contains Dopamine Hydrochloride and some other additives such as Dextrose, Sodium Metabisulfite, and may contain Hydrochloric Acid and/or Sodium Hydroxide for adjustment. The medication is meant for intravenous usage only and the usual dosage is shown on the insert included in the pack. It is manufactured by Hospira Inc. and contains Sulfites. It is not recommended to add any drug additives to the pack, and it must not be used in series connections. For more information, refer to the insert.*

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Principal Display Panel (500 mL Bag Label)

TO OPEN — TEAR AT NOTCH This text describes the usage, dosage and precautions of an injectable solution containing dopaine yirochirids, dotrosa and Iyorous, and may also contain hysrochioric acd and/or sodum hysroide. The solution is packaged in a single-dose container and is for intravenous use only. The user must check the package for damages or leaks before use, and promptly use the solution. It should be stored at 20-25°C and protected from freezing. The text also warns that the solution contains sulfites, and drug additives should not be made to the solution.*

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Principal Display Panel (500 mL Bag Label)

This is a drug description of a Dopamine HCI in 5% Dextrose Injection, USP. Each 100 mL contains Dopamine Hydrochloride 160 mg and Dextrose, Anhydrous 5 g in water for an injection. The drug additive should not be made to this solution. The solution is sterile, non-pyrogenic, and must not be used in series connections. Single-dose container discard unused portions. WARNING: Contains sulfites. The manufacturer is Hospira NG, Lake Forest.*

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Principal Display Panel (250 mL Bag Label)

The text describes instructions, dosage, and warnings for a medication contained in a single-dose container. The medication is called cortans dopamine, and the container comes in a 250 mL size. The instructions outline how to open the container, use the medication, and how to store it. The medication contains sulfates and should not be used if the overwrap is damaged or if the solution is discolored or cloudy.*

FDA Label Image

Principal Display Panel (250 mL Bag Label)

This is a description of a medication called Dopamine HCI. It comes in a 250mL injection bottle and is mixed with 5% Dextrose. The concentration is 800mg/250 mL. The text warns that the medication contains sulfites and provides dosage information on an insert. The medication is prescription only, and it is distributed by Hospira in Lake Forest, Illinois, USA.*

* 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.