Methylprednisolone Sodium Succinate Injection
Product Images NDC 51662-1695

View Photos of Packaging, Regulatory Labels, and Product Appearance

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 (51662 1695 Source Drug)
This product is a medication that needs to be reconstituted with 2 mL of Water for Injection or Bacteriostatic. It contains Sodium Succinate methylprednisolone sodium succinate, equivalent to 125 mg of methylprednisolone when reconstituted. The medication is lyophilized in a container and needs to be protected from light. The recommended dosage and usage instructions should be followed as per the prescribing information. It is intended for intramuscular or intravenous use only. The product is manufactured by Tianjin Kingyork Pharmaceuticals in Tianjin, China, and distributed by Dr. Reddy's Laboratories, Inc.*
FDA Label Image

Structure (51662 1695 Structure)

FDA Label Image

Label (51662 1695 1 Rfid)

Label (51662 1695 1 Rfid)
This is a product label containing a series of numbers and contact information for the manufacturer. It also mentions that the product is for prescription use only. The product is distributed by HF Acquisition Co., LLC located in Mukilteo, WA 98275. For more details about the product, it advises checking the manufacturer's insert.*
FDA Label Image

Label (51662 1695 2 Pouch)

Label (51662 1695 2 Pouch)
This text appears to be a description of a medication product named "METHYLPREDNISOLONESODIUMSUCCINATE INJECTION, USP 125mg VIAL." The text includes details such as NDC number, LOT number, expiration date, dosage instructions, storage information, and components of the medication. The medication is in the form of a single-dose vial and does not contain diluent. It contains methylprednisolone sodium succinate equivalent to a certain dosage. It also mentions the presence of specific components like monobasic sodium phosphate, dibasic sodium phosphate dried, and sodium hydroxide. The product is designed for intravenous use only. The manufacturer's package insert likely provides more detailed information.*
FDA Label Image

Label (51662 1695 3 Case)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.