Product Images Dopamine Hydrochloride

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Product Label Images

The following 10 images provide visual information about the product associated with Dopamine Hydrochloride NDC 51662-1316 by Hf Acquisition Co Llc, Dba Healthfirst, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

BAG LABEL - CONTAINER LABEL

BAG LABEL - CONTAINER LABEL

This is a medication called Dopamine HCI with 160 mg of dopamine hydrochloride and 5 g of dextrose, hydrous in each 100 mL. It is used for intravenous injection and contains sodium metabisulfite as an additive. The container is for single use only, and any unused portion should be discarded. The medication should be used promptly after the overwrap is opened, and if there are any defects or darkening, it should also be discarded. It should be stored at controlled room temperature and protected from freezing. The medication is manufactured by Hospira, Inc.*

DOSAGE 1 - DOSAGE AND ADMINISTRATION 1

DOSAGE 1 - DOSAGE AND ADMINISTRATION 1

DOSAGE 2 - DOSAGE AND ADMINISTRATION 2

DOSAGE 2 - DOSAGE AND ADMINISTRATION 2

DOSAGE 3 - DOSAGE AND ADMINISTRATION 3

DOSAGE 3 - DOSAGE AND ADMINISTRATION 3

HOW SUPPLIED - HOW SUPPLIED

HOW SUPPLIED - HOW SUPPLIED

This is a product description of Total Strength/Total Unit of Sale Volume available in different concentrations and sizes with NDC codes. It is a medication that comes in a carton and is available in different strengths as specified by the concentration in each carton. However, the has made a mistake in interpreting some characters resulting in the appearance of 'mcg/mlL' and 'meg/ml' which may not be accurate.*

LOGO - LOGO

LOGO - LOGO

PRECAUTIONS - PRECAUTIONS

PRECAUTIONS - PRECAUTIONS

This text provides important information on how to prevent tissue damage in ischemic areas. To do so, it suggests promptly infiltrating the affected area with a solution of 0.9% Sodium Chloride Injection, USP, containing 5 to 10 mg of Regitine (phentolamine), an adrenergic blocking agent. It also notes that the recommended pediatric dosage of Regitine is 0.1-0.2 mg/kg up to a maximum of 10 mg per dose. To administer the solution, a fine hypodermic needle should be used, and it should be widely infiltrated throughout the ischemic area. The text also explains that administering phentolamine in this way causes immediate and noticeable changes in the affected area, so it is important to do so as soon as possible after noticing any symptoms.*

SERIALIZED LABELING - SERIALIZED LABEL RESIZED

SERIALIZED LABELING - SERIALIZED LABEL RESIZED

STRUCTURE 1 - STRUCTURE 1

STRUCTURE 1 - STRUCTURE 1

STRUCTURE 2 - STRUCTURE 2

STRUCTURE 2 - STRUCTURE 2

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.