Methylprednisolone Acetate Injection, Suspension
Product Images NDC 60219-1573

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Acetate (NDC 60219-1573). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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

1 (Methylprednisolone Acetate Injectable Suspension U 1)

Chemical structure diagram of methylprednisolone acetate showing the steroid backbone with various functional groups including hydroxyl, keto, and acetate ester substituents.*

FDA Label Image

2 (Methylprednisolone Acetate Injectable Suspension U 2)

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension U 3)

Label for Methylprednisolone Acetate Injectable Suspension, USP 40 mg/mL, 1 mL single-dose vial. The label indicates it is for intramuscular, intrasynovial, and soft tissue injection only, not for intravenous use. Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ, made in India, with barcode and lot/expiration area.*

FDA Label Image

2 (Methylprednisolone Acetate Injectable Suspension U 4)

Label for Methylprednisolone Acetate Injectable Suspension, USP 40 mg/mL by Amneal Pharmaceuticals NY LLC. The label indicates a 1 mL single-dose vial for intramuscular, intrasynovial, and soft tissue injection only, not for intravenous use. It includes storage instructions and manufacturer details from Amneal Pharmaceuticals Pvt. Ltd., India, and distribution by Amneal Pharmaceuticals LLC, Bridgewater, NJ.*

FDA Label Image

3 (Methylprednisolone Acetate Injectable Suspension U 5)

Packaging label for Methylprednisolone Acetate Injectable Suspension, USP 40 mg/mL by Amneal Pharmaceuticals NY LLC. The label indicates the product is for intramuscular, intrasynovial, and soft tissue injection only, not for intravenous use. It contains 26 single-dose vials of 1 mL each and features storage instructions alongside manufacturer and distributor details.*

FDA Label Image

4 (Methylprednisolone Acetate Injectable Suspension U 6)

Label for Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, in a 1 mL single-dose vial. The label includes usage routes (intramuscular, intrasynovial, and soft tissue injection), highlights dosage and usage instructions, and lists Amneal Pharmaceuticals LLC as the distributor with manufacturing in India. The label features the Premier ProRx branding and a barcode.*

FDA Label Image

5 (Methylprednisolone Acetate Injectable Suspension U 7)

Packaging label for Methylprednisolone Acetate Injectable Suspension USP, 80 mg/mL. The product is an injection suspension for intramuscular, intra-articular, intralesional, and soft tissue use only, not for intravenous use. The label indicates a 1 mL single-dose vial, manufactured by Amneal Pharmaceuticals NY LLC with manufacturing by Amneal Pharmaceuticals Pvt. Ltd. in India, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. The label includes dosage, storage instructions, barcode, and trademark PREMIEProRx.*

FDA Label Image

6 (Methylprednisolone Acetate Injectable Suspension U 8)

Packaging label for Methylprednisolone Acetate Injectable Suspension USP 80 mg/mL from PremierProRx. The label indicates use for intramuscular, intranasal, and soft tissue injection only, not for intravenous use. Contains 25 single-dose vials of 1 mL each. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC.*

* 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.