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

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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)

Vial (1000670 0009 0039 30 Solu Medrol Vial Label)
This is a single-use vial of Act-0-Vial®, containing methylprednisolone for intramuscular or intravenous use only. It is important to discard any unused portion of the vial and to protect it from light. The dosage and use should be determined by the prescribing medical professional. Each mL of the vial contains 40 mg of methylprednisolone. This product is distributed by Pharmacia & Upjohn Co, a division of Pfizer Inc, and is preservative-free. NDC code for this product is 0008-0039-30.*
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Serialized Label (51662 1264 1 Solumedrol 40 Serialized Label)

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5166212642 Label

5166212642 Label
This is a medication with the NDC code 51662-1264-2. The LOT number is ABCDEFGHIJKLMNOP@QRST and the expiration date is 2021-06-D1. The medication should be stored at room temperature and protected from light. It is for intravenous or intramuscular use only and any unused portion should be discarded. The manufacturer is referenced, along with a distributor located in Mukilteo, WA 98275.*
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5166212643 Rfid Label

FDA Label Image

5166212643 Label

5166212643 Label
Solu-Medrol® is a medication available in a 40mg per vial 1mL box of 25, with NDC number 51662-1264-3. The specific lot number is ABCDEFGHIJKLMNOPQRST, with expiration date 2021-06-01. The medication is for intramuscular or intravenous use only and should be discarded if unused. It should be stored at controlled room temperature, between 20°C to 25°C (68°F to 77°F), and protected from light. The manufacturer's package insert is available to consult. The original manufacturer's NDC is 0009-0039-30. This medication is distributed by HF Acquisition Co., LLC in Mukilteo, WA 98275.*
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Dosage Image (Dosage Image)

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Dosage (Dosage Table)

Dosage (Dosage Table)
This text appears to be a list of different types of corticosteroids with their respective dosages. It can be used as reference material for medical purposes.*
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Supplied 1 (How Supplied 1st)

Supplied 1 (How Supplied 1st)
This text appears to be a list of different vial sizes and their corresponding NDC codes (National Drug Code). It includes a 500mg and 1 gram multi-dose vial, an 8 ml vial with NDC code 0009-0758-01 and a 16 ml vial with NDC code NPC0009-0698-. Lastly, there is a 2 gram vial that comes with diluent and has NDC code 0009-0796-01. It is possible that this information is related to medication or pharmaceuticals, but without more context it is difficult to say for certain.*
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Supplied 2 (How Supplied 2nd)

Supplied 2 (How Supplied 2nd)
This is a description of different Act-O-Vial System presentations, varying in their dosage, which consist of single-use vials with different quantities ranging from 40mg to 500mg. The vials are available in different sizes, such as 1 gram, 2 mL, 4 mL, and 8 mL, and have specific NDC numbers for identification purposes.*
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Logo (Logo)
G2 rectavies is a product distributed by Pharmacia & Upjohn Co, which is a division of Pfizer Inc, located in New York, NY 10017.*
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Preservative Free (Preservative Free)

Preservative Free (Preservative Free)
The text describes Act-O-Vial System, a product available in different doses, each containing methylprednisolone sodium succinate as the active ingredient, along with other ingredients. The doses available are 40mg, 125mg, 500 mg, and 1 gram. The product comes in Single-Use Vials and needs to be mixed for administration.*
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Preservative (Preservative)

Preservative (Preservative)
This text describes the composition of three different packages of SOLU-MEDROL. The 500 mg and 1 gram vials contain methylprednisolone sodium succinate, a type of corticosteroid drug, as well as two types of sodium phosphate. These packages do not contain a diluent and therefore, Bacteriostatic water is recommended as a diluent. However, the diluent contains benzyl alcohol, which acts as a preservative. The 2 gram vials come with a packaged diluent containing benzyl alcohol, and when mixed as directed, provide 2 grams of methylprednisolone. Users are cautioned to use only the recommended diluent or Bacteriostatic Water with Benzyl Alcohol for injecting SOLU-MEDROL, and to use it within 48 hours after mixing.*
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Structure (Structure Image)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.