Methylprednisolone Acetate Injection, Suspension
Product Images NDC 55150-313

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Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Acetate (NDC 55150-313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel-400 mg Per 10 mL (40 mg/ml) (Container Label)

Package Label-principal Display Panel-400 mg Per 10 mL (40 mg/ml) (Container Label)
This is a prescription drug with the NDC number 55150-313-01. It contains MethyIPREDNISolone Acetate and Benzyl Alcohol as a preservative. The dosage and usage instructions are available in the insert provided along with the drug. It is suggested to shake the suspension well before use. This drug is manufactured in India for Eugia US LLC and is not meant for IV use. The drug comes in a sterile 10 mL vial with a batch number and an expiration date mentioned.*
FDA Label Image

Package Label-principal Display Panel-400 mg Per 10 mL (40 mg/ml) (Container-Carton (1 Vial))

Package Label-principal Display Panel-400 mg Per 10 mL (40 mg/ml) (Container-Carton (1 Vial))
This is a pharmaceutical product with the name Methylprednisolone Acetate Injectable Suspension. It is available in a 10 mL multiple-dose vial containing 400 mg of the active ingredient. The usual dosage is provided with the accompanying prescribing information. It should be shaken well before use and is intended for intramuscular, intrasynovial, and soft tissue injection only, and not for intravenous use. It contains benzyl alcohol as a preservative, and the vial stopper is not made with natural rubber latex. The product is distributed by Eugia US LLC and made in India.*
FDA Label Image

Package Label-principal Display Panel-400 mg Per 10 mL (40 mg/ml) (Container-Carton (25 Vials))

Package Label-principal Display Panel-400 mg Per 10 mL (40 mg/ml) (Container-Carton (25 Vials))
This is a description of a medication named Methylprednisolone Acetate. It is an injectable suspension with 400 mg per 10 mL (40 mg/mL) that is for intramuscular, intrasynovial, and soft tissue injection only. This medication contains benzyl alcohol as a preservative and is supplied in sterile 25 x 10 mL multiple-dose vials. The usual dosage is not given, and it is recommended to see accompanying prescribing information. The medication should be shaken well before each use, and it should be stored between 20° to 25°C (68° to 77°F). The vial stopper is not made with natural rubber latex. The medication is distributed by Eugia US LLC and is made in India.*
FDA Label Image

Package Label-principal Display Panel-400 mg Per 5 mL (80 mg/ml) (Container Label)

Package Label-principal Display Panel-400 mg Per 5 mL (80 mg/ml) (Container Label)
This is a prescription drug with the NDC number 55150-314-01. It contains benzyl alcohol as a preservative. The usual dosage and other important information can be found in the insert. This is an injectable suspension for IM, intrasynovial and soft tissue injection only, and not for IV use. The pack contains a 5 mL multiple-dose vial. However, the batch number, expiration date, and other information are not available.*
FDA Label Image

Package Label-principal Display Panel-400 mg Per 5 mL (80 mg/ml) (Container-Carton (1 Vial))

Package Label-principal Display Panel-400 mg Per 5 mL (80 mg/ml) (Container-Carton (1 Vial))
The text describes a medication called Methylprednisolone Acetate Injectable Suspension, USP with a strength of 400mcg per 5mL. It is a sterile multiple-dose vial intended for intramuscular, intrasynovial and soft tissue injection only, and should not be used intravenously. The medication contains Benzyl Alcohol as a preservative and should be shaken well before use. Each mL contains methylprednisolone acetate, USP, 80 mg, along with several other ingredients. The usual dosage information is available with the accompanying prescribing information. The vial stopper is not made with natural rubber latex. The medication is distributed by Eugia USLLC and made in India.*
FDA Label Image

Package Label-principal Display Panel-400 mg Per 5 mL (80 mg/ml) (Container-Carton (25 Vials))

Package Label-principal Display Panel-400 mg Per 5 mL (80 mg/ml) (Container-Carton (25 Vials))
The text is a description of a medication called Bicso methylPREDNISolone Acetate, it is an Injectable Suspension with 400 mg per 5 mL (80 mg/mL) for intramuscular, intrasynovial and soft tissue injection only, it contains Benzyl Alcohol as a preservative and it comes in sterile 25 x 5 mL Multiple-Dose Vials. The usual dosage and instructions are not available. It should be stored at temperatures 20° to 25°C (68° to 77°F) and the vial stopper is not made with natural rubber latex. This medication is distributed by Eugia USLLC in Princeton-Hightstown, NJ, and it is made in India.*
FDA Label Image

Methylprednisolone Acetate Chemical Srtucture (Methylprednisolone Str)

Methylprednisolone Acetate Chemical Srtucture (Methylprednisolone Str)

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