Methylprednisolone Sodium Succinate Injection
Product Images NDC 51662-1695

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Sodium Succinate (NDC 51662-1695). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Label (51662 1695 Source Drug)

Label for methylprednisolone sodium succinate injection, USP, 125 mg per vial. The label states it is for intramuscular or intravenous use only, single dose vial, discard unused portion. It includes reconstitution instructions and manufacturer details: Tianjin Kingyork Pharmaceuticals Co., Ltd. (Tianjin, China), distributed by Dr. Reddy's Laboratories, Inc., Princeton, NJ, USA.*

FDA Label Image

Structure (51662 1695 Structure)

Chemical structure diagram of methylprednisolone sodium succinate, showing its steroid backbone with various functional groups including hydroxyl, ketone, and carboxylate components.*

FDA Label Image

Label (51662 1695 1 Rfid)

The image shows a white pharmaceutical label with a barcode and a QR code, including numeric codes such as (01)00351662169513 and others. It states the product is distributed by HF Acquisition Co., LLC in Mukilteo, WA 98275, with a note to see the manufacturer's insert. No brand name, dosage strength, or dosage form is visible on this label.*

FDA Label Image

Label (51662 1695 2 Pouch)

Label for Methylprednisolone Sodium Succinate injection, USP 125 mg vial. The label includes the NDC 51662-1695-2, lot number, and expiration date. It specifies single-dose vial use without diluent and storage instructions at controlled room temperature. Distributed by HF Acquisition Co, LLC, Mukilteo, WA.*

FDA Label Image

Label (51662 1695 3 Case)

Label for Methylprednisolone Sodium Succinate injection, USP 125 mg single-dose vial, packaged in a case of 25. Includes NDC 51662-1695-3, lot number 789210, and expiration date 2030-09-19. Distributed by HF Acquisition Co., LLC, Mukilteo, WA. Label provides preparation and storage instructions and notes it contains no diluent.*

* 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.