Product Images Methylprednisolone Sodium Succinate

Succinate for Injection, USP is a medication distributed by GeneYork Pharmaceuticals in SOL, WIS USA. Each vial contains 125 mg and is safe for intramuscular or intravenous use. It is recommended to use each vial as a single dose and discard any unused contents.*

This is a description of a medication called MethylPREDNISolone Sodium Succinate, which is available in a single-dose vial containing 125mg per vi. The medication is for intramuscular or intravenous use only, and should be used as per accompanying prescribing information. The medication should be reconstituted with 2 mL of Water for Injection or Bacteriostatic Water for Injection with Benzyl Alcohol. Each 2 mL of reconstituted solution contains methylprednisolone sodium succinate, equivalent to 125mg of methylpredisolone. The medication is lyophilized in a container and should be protected from light. Unused portion of the medicine should be discarded. The remaining text describes the manufacturer details and revision information, along with a barcode.*

This is a product description and usage instructions for Methylprednisolone Sodium Succinate Injection, USP. This medication is administered through intramuscular or intravenous injection and comes in a 1 g vial. The usual recommended dosage is not clear. The medication should be stored in a controlled room temperature, protected from light, and kept away from children. The product has a lot number and an expiration date.*

This is a package information for Methylprednisolone, a medication used to treat inflammation, allergic reactions, and certain types of cancer. The package contains a vial of Sodium Succinate 3% and needs to be reconstituted with 16 mL Bacteriostatic Water for Injection, USP, before intravenous administration. The usual dose should be determined by a healthcare professional, according to the prescribing information. It should be stored at a controlled room temperature and protected from light. The package is distributed by GeneYork Pharmaceutical Group and manufactured in China.*

This is a description for a medication and its storage instructions. The label provides details for two forms of an injection: Methylprednisolone Sodium Succinate for Intramuscular or Intravenous use. The medication needs to be stored in a controlled environment with a temperature range between 65 to 77 degrees Fahrenheit. The packaging contains individual single-dose vials that must be disposed of if unused. The label indicates the manufacturer's location, product name, and recommended dosage.*

This is a description of a medication called MethylPREDNISolone Sodium Succinate for Injection, which is only for intramuscular or intravenous use. It is available in a single-dose vial with instructions to discard any unused portion. The package does not come with a diluent, but it is recommended to be diluted with Bacteriostatic Water for Injection that contains Benzyl Alcohol as a preservative. The medication should be stored at a temperature range of 20°C to 25°C and protected from light. The medication contains methylprednisolone, and the usual dosage instructions are provided in the accompanying prescribing information. The medication is manufactured by GeneYork Pharmaceuticals Group LLC and is made in China.*

This appears to be a label of a medication called "methylPREDNISolone Sodium Succinate for Injection, USP" with a recommended dosage. The medication is meant for intramuscular or intravenous use only. The label also includes a warning to discard any unused portion of a single-dose vial.*

This appears to be a label of a pharmaceutical product that is manufactured in China and distributed by a company named GensYork Pharmaceuticals LLC based in the USA. The product is intended for intramuscular or intravenous use only and it is packaged in single-dose vials. The label also includes the recommended disposal instructions for any unused portion of the product. Lastly, the label dimensions are provided as 117mm x 117mm x 50mm.*

This is a description for a medication that is to be reconstituted with 1 mL of water for injection or Baerosiaic water for injection, and contains methylPREDNISolone Benzyt Alcohol Sodium Succinate. Each mL, when reconstituted, contains methyliprenisolone sodium succinate for Injection, USP CquAT 1o methylprecnSoone. It is for intramuscular or intravenous use only and is a single-dose vial. The medication is lyophilized in a container and should be protected from light. The prescription information is available and the dosage is based on the physician's recommendation. Finally, there is no information about the medication's lot or expiration date.*

Sodium Succinate for Injection, USP is a medication administered intravenously in the treatment of certain medical conditions. Each vial contains 500 g of the active ingredient. The dimensions of the vial are 35x35x82mm.*

This is a medication label for NDC 71329-303-01 containing instructions on how to reconstitute the medication by mixing it with 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol. The medication should be protected from light and stored at a controlled room temperature of 20° to 25°C (68° to 77°F). The usual dosage is 500mg per vial, and once reconstituted, the resultant concentration is 625mg per mL for intramuscular or injection use only. The medication is lyophilized in a container, and the package does not contain a diluent. The accompanying prescribing information should be consulted for usual dosage and administration instructions.*