Dexmedetomidine Injection, Solution
Product Images NDC 71288-505

3 FDA label images from Meitheal Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine (NDC 71288-505). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Dex18 0000 01)

Structural Formula (Dex18 0000 01)
Chemical structure of dexmedetomidine hydrochloride, showing a benzene ring with methyl groups, an imidazole ring, and the associated hydrochloride (HCl) component as part of the molecular structure.*
FDA Label Image

Principal Display Panel – Dexmedetomidine Injection, Usp 200 Mcg Per 2 mL Vial Label (Dex18 0000 02)

Principal Display Panel – Dexmedetomidine Injection, Usp 200 Mcg Per 2 mL Vial Label (Dex18 0000 02)
Label for Dexmedetomidine Injection, USP, containing 200 mcg per 2 mL (100 mcg per mL) for intravenous use. The label indicates it must be diluted and comes in a 2 mL single-dose vial. Manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, USA. The label includes NDC 71288-505-02 and shows space for lot and expiration details.*
FDA Label Image

Principal Display Panel – Dexmedetomidine Injection, Usp 200 Mcg Per 2 mL Carton (Dex18 0000 03)

Principal Display Panel – Dexmedetomidine Injection, Usp 200 Mcg Per 2 mL Carton (Dex18 0000 03)
Box packaging label for Dexmedetomidine Injection, USP 200 mcg per 2 mL (100 mcg per mL) for intravenous use. The box contains 25 single-dose vials of 2 mL each. Labeler is Meitheal Pharmaceuticals Inc. The label includes storage instructions, dosage form, and a statement that the solution must be diluted before use.*

* 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.