Methylprednisolone Sodium Succinate Injection
Product Images NDC 70518-3684

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Sodium Succinate (NDC 70518-3684). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
This is a description for a medication called methylPREDNISolone Sodium Succinate. Each vial contains 125mg of the medication and there are 25 vials in a package. This medication is intended for intramuscular or intravenous use only. It should be protected from light and is a single-dose vial. Any unused portion should be discarded. The medication is available by prescription only. The NDC number for this medication is 70518-3684-00. The expiration date and lot number are not available. The manufacturer is Dr. Reddy's, located in Shreveport, LA 71106. It is important to keep this medication and all medications out of the reach of children. Reconstitution of the medication should be done with either 2mL Water for Injection or Bacteriostatic Water for Injection with Benzyl Alcohol. The directions for use can be found in the package insert. It should be stored at a temperature of 20-25°C (88-77°F), with permitted excursions between 15-30°C (59-86°F) [See USP]. The medication has been repackaged by RemedyRepack Inc., located in Indiana, PA 15701.*
FDA Label Image

Mm2 (Methylprednisolone Sodium Succinate 125mgper Vial 70518 3684 01)

Mm2 (Methylprednisolone Sodium Succinate 125mgper Vial 70518 3684 01)
This is a description for a medication called methylPREDNISolone Sodium Succinate. It comes in a vial with 125mg of the medication. The vial contains 12mL of the injection. This medication is meant for intramuscular or intravenous use only and should be protected from light. It is a single-dose vial and any unused portion should be discarded. The medication comes with specific instructions for reconstitution using either 2mL of Water for Injection or Bacteriostatic Water for Injection with Benzyl Alcohol. The package insert provides directions for use. The medication should be stored at a temperature of 20-25°C (88-77°F) with excursions permitted between 15-30°C (59-86°F) according to USP standards. The medication is repackaged by RemedyRepack Inc. in Indiana, PA.*
FDA Label Image

Structure (Structure)

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