Dextrose Monohydrate Injection, Solution
Product Images NDC 51662-1453
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dextrose Monohydrate (NDC 51662-1453). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hf Acquisition Co Llc, Dba Healthfirst, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Alternate Superseeded Syringe Labeling (Alternate Superseeded Syringe Labeling)
50% DEXTROSE Inj, usp is a sterile, nonpyrogenic solution used for L.V. administration. It contains 25 grams (0.5 g/mL) of dextrose and is packaged in 50mL single-dose vials with NDC 0409-4902-34. The usual dosage and other information can be found in the insert. The solution has a pH of 4.2 and a calculated osmolality of 253 mOsmol/mL. It is manufactured by Hospira, Inc., located in Lake Forest, IL, USA.*
Carton Label (Carton Label)
How Supplied (How Supplied)
This is a description of different pharmaceutical products which are sold in units of concentration. It includes details about the packaging of each product, such as the size and quantity of syringes or vials contained in each bundle or tray. The products are identified by their NDC (National Drug Code) numbers, which are used to ensure they are accurately identified and billed.*
Logo (Logo)
Serialized Labeling (Serialized Labeling)
Structure (Structure)
Syringe Label (Syringe Label)
This is a description of a medication called "50% Dextrose Injection". It comes in a single dose of 50 mL, and is only for intravenous use. The medication contains 25 g of dextrose in a 50 mL solution (0.5 g/mL). The usual dosage instructions are not provided. The medication is described as sterile and non-pyrogenic, and has a calculated osmolality of 253 mOsmol/L. The pH is listed as 4.2. The medication is produced by Hospira, located in Lake Forest, USA.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.