Solu-medrol Injection, Powder, For Solution
Product Images NDC 51662-1263

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Solu-medrol (NDC 51662-1263). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co. Llc, Dba Healthfirst, 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

Vial (1000660 0009 0047 25 Solu Medrol Vial Label)

Solu-Medrol 125 mg injection powder vial label for intramuscular or intravenous use. The label states 2 mL Act-O-Vial contains methylprednisolone sodium succinate for injection, preservative-free. It includes handling instructions, dosage form, and distributor information (Pharmacia & Upjohn Co, Pfizer). The National Drug Code (NDC) 0009-0047-25 appears on the label.*

FDA Label Image

Serialized Label (51662 1263 1 Solumedrol 125 Serialized Label)

SOLU-MEDROL 125 mg/2 mL injection powder for solution in a clear glass vial with an orange flip-off cap. The vial has a white label including barcodes and text indicating distribution by HF Acquisition Co., LLC. The label also instructs to see the manufacturer's package insert and notes the product is for prescription use only.*

FDA Label Image

5166212632 Label

Label for SOLU-MEDROL 125 mg per vial, 2 mL injection powder for solution. The label shows the NDC number 51662-1263-2 and contains lot number and expiration date 2021-06-01. The product is indicated for intramuscular or intravenous use and is distributed by HF Acquisition Co., LLC in Mukilteo, WA. The label includes storage instructions and a QR code.*

FDA Label Image

5166212633 Rfid Label

A small rectangular pharmaceutical label contains a GS1 DataMatrix barcode and several lines of numeric and alphanumeric text. The text includes application identifiers such as (01) 00351662126332, (17) 210601, (21) 12345, and (10) ABC123. It instructs to see the manufacturer's package insert and states the product is distributed by HF Acquisition Co., LLC, Mukilteo, WA 98275. The label also has "RX ONLY" printed vertically on the right side.*

FDA Label Image

5166212633 Label

Label for SOLU-MEDROL 125 mg per vial 2 mL injection powder for solution, packaged as a box of 25 vials. The label shows the product NDC 51662-1263-3, a lot number placeholder, and an expiration date of 2021-06-01. The label indicates the product is for intramuscular or intravenous use only and is distributed by HF Acquisition Co., LLC, Mukilteo, WA.*

FDA Label Image

Needle (Dosage Image)

An instructional diagram illustrating the correct technique for inserting a needle through the rubber stopper of a vial, showing the needle penetrating the stopper, designed to support proper medication preparation procedures.*

FDA Label Image

Dosage (Dosage Table)

A data table listing corticosteroid types and numerical values associated with each: Cortisone 25, Hydrocortisone 20, Prednisolone 5, Prednisone 5, Methylprednisolone 4, Triamcinolone 4, Paramethasone 2, Betamethasone 0.75, and Dexamethasone 0.75.*

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How Supplied 1 (How Supplied 1st)

A data table displaying different vial sizes and NDC codes for an unspecified drug. The left side lists a 500 mg multi-dose vial with 8 mL volume and its NDC 0009-0758-01. The right side lists a 1 gram multi-dose vial with 16 mL and NDC 0009-0698-01, and a 2 gram vial with diluent with NDC 0009-0796-01.*

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How Supplied 2 (How Supplied 2nd)

A data table listing different sizes and NDC codes of Act-O-Vial System single-use vials. It includes 40 mg vials (25 x 1 mL), 125 mg vials (25 x 2 mL), 500 mg vials (4 mL), and a 1 gram vial (8 mL), each with their respective NDC codes.*

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Logo (Logo)

FDA Label Image

Preservative Free (Preservative Free)

This text panel lists the composition details for various methylprednisolone sodium succinate powder for solution injections called Act-O-Vial System, available in single-use vials of 40 mg, 125 mg, 500 mg, and 1 gram strengths. It specifies the quantity of methylprednisolone and accompanying excipients like monobasic sodium phosphate anhydrous and dibasic sodium phosphate dried per vial.*

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Preservative (Preservative)

Drug text panel describing composition and instructions for SOLU-MEDROL injection powder for solution, listing available vial sizes (500 mg, 1 gram, 2 gram with diluent) with methylprednisolone sodium succinate content and preservative information. Includes guidance on recommended diluent (Bacteriostatic Water containing benzyl alcohol) and storage post-mixing.*

FDA Label Image

Structure (Structure Image)

Chemical structure diagram of the active ingredient solumedrol, showing the steroid backbone with functional groups including hydroxyl and ketone substituents, and a sodium salt ester side chain.*

* 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.