Methylprednisolone Sodium Succinate Injection, Powder, Lyophilized, For Solution
Product Images NDC 70121-1001

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Sodium Succinate (NDC 70121-1001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, 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

1 (Methylprednisolone Sodium Succinate For Injection 1)

Chemical structure of methylprednisolone, showing its steroid backbone with associated functional groups, including hydroxyl, carbonyl, and sodium succinate moieties.*

FDA Label Image

1 (Methylprednisolone Sodium Succinate For Injection 2)

Label of Methylprednisolone Sodium Succinate for Injection, USP, 40 mg per vial, 1 mL single-dose vial for intramuscular or intravenous use. Contains lyophilized powder to be reconstituted with bacteriostatic water containing benzyl alcohol. Distributed by Amneal Pharmaceuticals LLC. Includes NDC 70121-1000-1 and handling instructions to protect from light.*

FDA Label Image

1 (Methylprednisolone Sodium Succinate For Injection 3)

Packaging label for Methylprednisolone Sodium Succinate 40 mg per vial injection, powder, lyophilized for reconstitution. The 1 mL single-dose vial is intended for intramuscular or intravenous use. Labeler is Amneal Pharmaceuticals LLC. The label includes storage instructions, NDC 70121-1000-5, and information about the diluent and usage.*

FDA Label Image

1 (Methylprednisolone Sodium Succinate For Injection 4)

Label for Methylprednisolone Sodium Succinate for Injection, USP, 125 mg per vial, 2 mL single-dose vial. It includes preparation instructions to reconstitute with 2 mL Sterile Water for Injection with Benzyl Alcohol preservative. The label states it is for intramuscular or intravenous use only, prescription only, and is distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ.*

FDA Label Image

1 (Methylprednisolone Sodium Succinate For Injection 5)

Methylprednisolone Sodium Succinate for Injection, USP 125 mg per vial powder label by Amneal Pharmaceuticals LLC. The label states the product is a single-dose vial containing 125 mg per 2 mL for intramuscular or intravenous use. It includes storage instructions and manufacturing information from Amneal Pharmaceuticals Pvt. Ltd.*

* 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.