Solu-medrol Injection, Powder, For Solution
Product Images NDC 51662-1264

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Solu-medrol (NDC 51662-1264). 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 (1000670 0009 0039 30 Solu Medrol Vial Label)

Label for Solu-Medrol 40 mg per vial injection, powder for solution, 1 mL Act-O-Vial. Contains methylprednisolone sodium succinate equivalent to 40 mg methylprednisolone. For intramuscular or intravenous use, preservative-free, Rx only. Distributed by Pharmacia & Upjohn Co, Pfizer division.*

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Serialized Label (51662 1264 1 Solumedrol 40 Serialized Label)

SOLU-MEDROL injection powder for solution vial showing a small clear glass vial with a red rubber stopper and a white plastic cap. The vial label includes barcodes, manufacturing and distribution information by HF Acquisition Co. LLC in Mukilteo, WA, and an instruction to see the manufacturer's package insert. The vial is for human prescription use.*

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5166212642 Label

Label for SOLU-MEDROL 40 mg per vial 1 mL ACT-O-VIAL injection powder for solution. Shows National Drug Code (NDC) 51662-1264-2, lot number represented as alphabetical sequence, and an expiration date of 2021-06-01. Indicates intramuscular and intravenous use and storage instructions. Distributed by HF Acquisition Co., LLC, Mukilteo, WA.*

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5166212643 Rfid Label

A product label with barcode and numeric codes including a GTIN starting with 00351662126431. It contains instructions to see the manufacturer\'s package insert and notes distribution by HF Acquisition Co. LLC, Mukilteo, WA 98275. The label includes a 'RX ONLY' indication, implying prescription drug status.*

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5166212643 Label

A label for SOLU-MEDROL 40 mg per vial, 1 mL ACT-O-VIAL, packaged in a box of 25. The label includes the NDC number 51662-1264-3, a placeholder lot number, and an expiration date of 2021-06-01. It also states that the product is for intramuscular or intravenous use, and is distributed by HF Acquisition Co., LLC, Mukilteo, WA 98275. A QR code is visible on the label.*

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Dosage Image (Dosage Image)

A technical line drawing illustrating a syringe needle inserted into a vial stopper, depicting the process of drawing medication or injection preparation.*

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Dosage (Dosage Table)

A table listing corticosteroid drugs alongside numerical values, including 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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Supplied 1 (How Supplied 1st)

A table displaying different vial sizes for a drug product, listing a 500 mg multi-dose vial with 8 mL volume and NDC 0009-0758-01, and a 1 gram multi-dose vial with 16 mL volume and NDC 0009-0698-01, as well as a 2 gram vial with diluent and NDC 0009-0796-01.*

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Supplied 2 (How Supplied 2nd)

A table listing various Act-O-Vial System single-use vial products with their strengths, quantities, and corresponding NDC codes. It includes 40 mg (25 x 1 mL), 125 mg (25 x 2 mL), 500 mg (4 mL), and 1 gram (8 mL) vial systems with specific NDC numbers for each.*

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Logo (Logo)

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Preservative Free (Preservative Free)

Text table listing the composition of SOLU-MEDROL Act-O-Vial Systems in various single-use vial strengths: 40 mg, 125 mg, 500 mg, and 1 gram methylprednisolone sodium succinate per vial when mixed. Each entry details the amount of methylprednisolone and accompanying sodium phosphate and lactose components per vial volume.*

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Preservative (Preservative)

Text panel describing different vial sizes of SOLU-MEDROL injection powder for solution, detailing methylprednisolone sodium succinate content per vial when mixed, along with monobasic sodium phosphate anhydrous and dibasic sodium phosphate dried amounts. It notes recommended diluent is bacteriostatic water containing benzyl alcohol as preservative, and instructions to use only the accompanying diluent or bacteriostatic water containing benzyl alcohol for reconstitution, with usage advised within 48 hours after mixing.*

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Structure (Structure Image)

Chemical structure of SOLU-MEDROL (methylprednisolone sodium succinate), showing the molecular arrangement of atoms and functional groups typical for this corticosteroid active ingredient.*

* 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.