Methylprednisolone Acetate Injection, Suspension
Product Images NDC 55150-314

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Acetate (NDC 55150-314). 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.

FDA Label Image

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

Methylprednisolone Acetate Injectable Suspension USP label for a 10 mL multiple-dose vial containing 40 mg/mL strength (total 400 mg per vial). The label indicates use for IM, intrasynovial, and soft tissue injection, not for IV use. It is labeled by Eugia US LLC and contains benzyl alcohol as a preservative. Batch and expiration date fields are blank.*

FDA Label Image

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

Packaging label for Methylprednisolone Acetate Injectable Suspension USP, 40 mg/mL strength (400 mg per 10 mL) in a sterile 10 mL multiple-dose vial. The label highlights it is for intramuscular, intrasynovial, and soft tissue injection only and contains benzyl alcohol as a preservative. Distributed by Eugia US LLC, made in India.*

FDA Label Image

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

Label for Methylprednisolone Acetate Injectable Suspension, USP 40 mg/mL (400 mg per 10 mL) by Eugia US LLC. The label specifies intramuscular, intrasynovial, and soft tissue injection routes only; not for intravenous use. Packaging indicates 25 x 10 mL multiple-dose vials. Contains benzyl alcohol as a preservative. Distributed by Eugia US LLC, made in India.*

FDA Label Image

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

Label for Methylprednisolone Acetate Injectable Suspension, USP, 80 mg/mL strength, supplied as 5 mL multiple-dose vial containing 400 mg per vial. Intended for intramuscular, intrasynovial, and soft tissue injection only, not for intravenous use. Manufactured in India for Eugia US LLC. Includes barcode and preservative information (benzyl alcohol).*

FDA Label Image

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

The packaging label for Methylprednisolone Acetate Injectable Suspension, USP, 80 mg/mL (400 mg per 5 mL) by Eugia US LLC. It is a sterile 5 mL multiple-dose vial for intramuscular, intrasynovial, and soft tissue injection, containing benzyl alcohol as a preservative. The label includes storage instructions, ingredients, and warnings, with a barcode and distributor information.*

FDA Label Image

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

Packaging label for Methylprednisolone Acetate Injectable Suspension USP, 80 mg/mL (400 mg per 5 mL) by Eugia US LLC. The label states the product is for intramuscular, intrasynovial, and soft tissue injection only, not for intravenous use. It contains benzyl alcohol as a preservative. The package includes 25 multiple-dose vials of 5 mL each. The label notes the product is sterile and provides storage instructions and ingredients details.*

FDA Label Image

Methylprednisolone Acetate Chemical Srtucture (Methylprednisolone Str)

Chemical structure of methylprednisolone acetate, a corticosteroid represented by its multi-ring steroidal backbone with functional groups including hydroxyl, ketone, and acetate moieties visible in the diagram.*

* 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.