Kit For The Preparation Of Technetium Tc 99m Medronate Injection, Powder, Lyophilized, For Solution
Product Images NDC 45567-0040

6 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Kit For The Preparation Of Technetium Tc 99m Medronate (NDC 45567-0040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Structural Formula (44b84192 4069 4300 9c17 54e31e949304 01)

Structural Formula (44b84192 4069 4300 9c17 54e31e949304 01)
Chemical structure of medronate, the active ingredient in Kit for the Preparation of Technetium Tc 99M Medronate. The diagram shows the molecular arrangement including phosphate groups and sodium ions, characteristic of this lyophilized injection compound.*
FDA Label Image

5 Vial Container (44b84192 4069 4300 9c17 54e31e949304 02)

5 Vial Container (44b84192 4069 4300 9c17 54e31e949304 02)
Label for Kit for the Preparation of Technetium Tc 99M Medronate for Injection, a sterile, diagnostic, multidose, non-pyrogenic lyophilized powder for solution. Each 10 mL vial contains 20 mg medronic acid with supporting ingredients. Manufactured by Sun Pharmaceutical Industries, Inc. Includes storage instructions, multidose vial details, and preparation notes.*
FDA Label Image

Pl-000010 (44b84192 4069 4300 9c17 54e31e949304 03)

Pl-000010 (44b84192 4069 4300 9c17 54e31e949304 03)
Packaging label for Kit for the Preparation of Technetium Tc 99M Medronate for Injection, a sterile diagnostic multidose, non-pyrogenic powder for solution. The label displays the Sun Pharma logo and includes content details, storage instructions, and manufacturer information for Sun Pharmaceutical Industries, Inc. The label notes the product is for intravenous use and contains reaction vials, medronic acid, ascorbic acid, and sodium fluoride in lyophilized form.*
FDA Label Image

Pl-000008 (44b84192 4069 4300 9c17 54e31e949304 04)

Pl-000008 (44b84192 4069 4300 9c17 54e31e949304 04)
Label for Kit for the Preparation of Technetium Tc99m Medronate for Injection, a sterile, diagnostic, multidose, non-pyrogenic powder for injection, lyophilized form. Each 10 mL multidose vial contains 20 mg medronic acid and other components. Manufactured by Sun Pharmaceutical Industries, Inc. The label includes storage instructions, recommended pH adjustments prior to lyophilization, and mentions use within 6 hours after reconstitution.*
FDA Label Image

30 Vial (44b84192 4069 4300 9c17 54e31e949304 05)

30 Vial (44b84192 4069 4300 9c17 54e31e949304 05)
Packaging label for Kit for the Preparation of Technetium Tc 99M Medronate for Injection by Sun Pharmaceutical Industries, Inc. The label indicates the product is a sterile, multidose, diagnostic, non-pyrogenic injection powder for intravenous use. The label includes handling instructions, storage conditions, and contact information for the manufacturer.*
FDA Label Image

Pl 000009 Rev 0.1.jpg.jpg.jpg.jpg

Pl 000009 Rev 0.1.jpg.jpg.jpg.jpg
Label of Kit for the Preparation of Technetium Tc 99M Medronate Injection, Powder, Lyophilized, for Solution, 20 mg/10 mL multidose vial. The label includes cautionary radioactive material symbol, formulation details, assay information, storage conditions, and manufacturer Sun Pharmaceutical Industries, Inc., Billerica, MA. It is indicated for diagnostic intravenous use with instructions for reconstitution and usage.*

* 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.