Methylprednisolone Acetate Injection, Suspension
Product Images NDC 70121-1609

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Methylprednisolone Acetate (NDC 70121-1609). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

Structure (Methylprednisolone Acetate Injectable Suspension 4 1)

Chemical structure of methylprednisolone acetate showing its steroid backbone with distinct functional groups, including hydroxyl and acetate moieties, depicted with solid and dashed bonds indicating stereochemistry.*

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension 4 2)

Methylprednisolone acetate injectable suspension, USP, 400 mg/10 mL (40 mg/mL) in a 10 mL multiple-dose vial. The label states it is for intramuscular, intrasynovial, and soft tissue injection only, contains benzyl alcohol as a preservative, and is distributed by Amneal Pharmaceuticals LLC. The label includes dosage instructions, storage conditions, and a barcode.*

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension 4 3)

Packaging label for Methylprednisolone Acetate Injectable Suspension, USP 400 mg/10 mL (40 mg/mL) by Amneal Pharmaceuticals LLC. The label indicates it is for intramuscular, intrasynovial, and soft tissue injection only, not for intravenous use. The 10 mL multiple-dose vial contains benzyl alcohol as a preservative. The label includes active and inactive ingredient information, manufacturer details, storage instructions, and a barcode.*

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension 4 4)

Packaging label for Methylprednisolone Acetate Injectable Suspension, USP 400 mg/10 mL (40 mg/mL) by Amneal Pharmaceuticals LLC. The label indicates intramuscular, intrasynovial, and soft tissue injection use only, not for intravenous use. It contains 25 multiple-dose vials of 10 mL each, with benzyl alcohol as a preservative. Storage instructions and inactive ingredients are also noted on the label.*

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension 4 5)

Label of Methylprednisolone acetate Injectable Suspension, USP 400 mg/5 mL (80 mg/mL) by Amneal Pharmaceuticals LLC. It is for intramuscular, intrasynovial, and soft tissue injection only. The label includes dosage form, strength, usage restrictions (not for intravenous use), storage instructions, manufacturer, distributor, NDC 70121-1610-1, and barcode. An area is designated for lot and expiration date.*

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension 4 6)

Packaging label for Methylprednisolone acetate Injectable Suspension, USP 400 mg/5 mL (80 mg/mL) by Amneal Pharmaceuticals LLC. It is a 5 mL multiple-dose vial for intramuscular, intrasynovial, and soft tissue injection only. Label states it is not for intravenous use and contains benzyl alcohol as a preservative. Instructions to shake well and storage temperature are included. The label includes NDC numbers and barcode.*

FDA Label Image

1 (Methylprednisolone Acetate Injectable Suspension 4 7)

Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL (400 mg/5 mL) vial label from Amneal Pharmaceuticals LLC. The label specifies the dosage form as injection suspension for intramuscular, intralesional, intrasynovial, intra-articular, and soft tissue use only, not for intravenous use. Packaging indicates 25 multiple-dose 5 mL vials. Contains benzyl alcohol as a preservative. Manufactured by Amneal Pharmaceuticals Pvt. Ltd., India, and distributed by Amneal Pharmaceuticals LLC, USA.*

* 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.