Midazolam Hydrochloride
Product Images NDC 68258-8973

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Midazolam Hydrochloride (NDC 68258-8973). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, 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.

FDA Label Image

Ndc 68258-8973-01 (Ndc 68258 8973 01 Hospira)

Ndc 68258-8973-01 (Ndc 68258 8973 01      Hospira)
This is a description of bulk-source data for a pharmaceutical product. The product is a Midazolam HCI injection in single-dose vials of 2mL each with a strength of either 5mg/mL or 6mg/mL. It is manufactured by Hospira, Inc. based in Lake Forest, IL 60045. The product information includes the NDC number, lot number, and pedigree number. The product must be stored between 68°-77° F and requires tight/light resistant container dispensing. Other information is provided on the package insert about the usual dosage, a black box warning, and medication disposal guidelines. The text also includes warnings and cautionary information about keeping the product out of children's reach, its habit-forming potential, and restrictions on transfer to a patient other than the one for whom it was prescribed.*
FDA Label Image

Structural Formula Midazolam (Midazolam Injection Usp3 Figure 1 Xen 2254 1)

FDA Label Image

Structural Formula Midazolam And Open-ring Form (Midazolam Injection Usp3 Figure 2 Xen 2254 2)

FDA Label Image

Graph Ph Dependence Of Open-ring Form In Water (Midazolam Injection Usp3 Figure 3 Xen 2254 3)

* 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.