Methylprednisolone Acetate
Product Images NDC 21695-849

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Acetate (NDC 21695-849). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Methylprednisolone Acetate Chemical Structure (Faf608f3 A13d 4969 B1a6 Bb0bc1de2a8e 01)

Chemical structure of Methylprednisolone Acetate showing its molecular framework with hydroxyl, ketone, and acetate functional groups clearly depicted in a steroid backbone arrangement.*

FDA Label Image

Methyprednisolone Acetate (40mg/ml) (Faf608f3 A13d 4969 B1a6 Bb0bc1de2a8e 02)

Label for Methylprednisolone Acetate Injectable Suspension (40 mg/ml) in a 10 ml vial. The label includes the NDC 21695-849-10 and indicates the product is distributed by Physician Partner and manufactured by Sandoz Canada Inc. It shows lot number, expiration date placeholders, and storage instructions to keep at controlled room temperature 15°-30°C. RX Only, Product ID RM084910 is also noted.*

FDA Label Image

Methyprednisolone Acetate (80mg/ml) (Faf608f3 A13d 4969 B1a6 Bb0bc1de2a8e 03)

Label for Methylprednisolone Acetate injectable suspension (80mg/ml) in a 5ml vial. The label shows the product name, strength, dosage form, and container size, with instructions to see the box for additional information. Distributed by Physician Partner, a division of Rebel Distributors Corp. Includes NDC code 21695-850-05 and identifies manufacturer as Sandoz Canada Inc. Contains lot and expiration placeholder text, storage instructions, and a red warning bar at the bottom.*

* 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.