Dexmedetomidine Hydrochloride Injection
Product Images NDC 52536-126

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Dexmedetomidine Hydrochloride (NDC 52536-126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wilshire 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.

FDA Label Image

Dexmed-structure (Dexmed Structure)

Dexmed-structure (Dexmed Structure)
Chemical structure diagram of dexmedetomidine hydrochloride showing the molecular framework including imidazole and aromatic ring components with attached functional groups.*
FDA Label Image

Dexmed 100ml Gland Dun Carton (Dexmed Glanddun 100ml Carton)

Dexmed 100ml Gland Dun Carton (Dexmed Glanddun 100ml Carton)
Packaging label for Dexmedetomidine Hydrochloride injection in 0.9% sodium chloride, 400 mcg/100 mL (4 mcg/mL) strength. The label states it is for intravenous infusion in single-dose bottles, packaged as 8 x 100 mL. Labeler is Wilshire Pharmaceuticals, Inc., with manufacturing by Gland Pharma Limited, India. Additional information includes storage conditions, dosage instructions, and preservative-free status.*
FDA Label Image

Dexmed 100ml Container Gland Dun (Dexmed Glanddun 100ml Container)

Dexmed 100ml Container Gland Dun (Dexmed Glanddun 100ml Container)
Label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg/100 mL (4 mcg/mL) strength in a 100 mL single-dose bottle. The label includes usage instructions for intravenous infusion, storage guidelines, and states the product is preservative-free. The manufacturer is Wilshire Pharmaceuticals, Inc.*
FDA Label Image

Dexmed 50ml Carton Gland Dun (Dexmed Glanddun 50ml Carton)

Dexmed 50ml Carton Gland Dun (Dexmed Glanddun 50ml Carton)
Packaging label for Dexmedetomidine Hydrochloride injection 4 mcg/mL (200 mcg/50 mL) in 0.9% Sodium Chloride. The product is a single-dose bottle for intravenous infusion, supplied in 10 x 50 mL bottles. Labeler is Wilshire Pharmaceuticals, Inc., with manufacturing by Gland Pharma Limited, Hyderabad, India. The label includes storage information and a barcode.*
FDA Label Image

Dexmed 50ml Container Gland Dun (Dexmed Glanddun 50ml Container)

Dexmed 50ml Container Gland Dun (Dexmed Glanddun 50ml Container)
Label for Dexmedetomidine Hydrochloride injection 4 mcg/mL in a 50 mL single-dose bottle. The label indicates this intravenous infusion contains 200 mcg per 50 mL. It includes storage instructions, preservative-free status, and is manufactured for Wilshire Pharmaceuticals, Inc. The label features a barcode and space for lot and expiration information.*
FDA Label Image

Dexmed 100ml Carton Gland Psm (Dexmed Glandpsm 100ml Carton)

Dexmed 100ml Carton Gland Psm (Dexmed Glandpsm 100ml Carton)
The packaging label for Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection shows an intravenous injection solution with a strength of 400 mcg/100 mL (4 mcg/mL). It is provided in single-dose 100 mL bottles, with an 8-count package by Wilshire Pharmaceuticals, Inc. The label includes dosage form, storage instructions, and manufacturing details.*
FDA Label Image

Dexmed 100ml Container Gland Psm (Dexmed Glandpsm 100ml Container)

Dexmed 100ml Container Gland Psm (Dexmed Glandpsm 100ml Container)
Label for Dexmedetomidine Hydrochloride 0.9% Sodium Chloride Injection, 400 mcg/100 mL (4 mcg/mL) for intravenous infusion. The single-dose 100 mL bottle label includes dosage strength, ingredients, storage instructions, and notes that it is preservative-free. Manufactured for Wilshire Pharmaceuticals, Inc., made in India.*

* 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.