Medrol
Product Images NDC 67296-1821

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Medrol (NDC 67296-1821). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Chemical Structure (Medrol 01)

Chemical structure diagram of the active ingredient in Medrol, showing a complex steroid framework with hydroxyl, carbonyl, and methyl groups attached, consistent with a corticosteroid compound.*

FDA Label Image

Logo (Medrol 02)

FDA Label Image

Principal Display Panel (4 mg Tablet Bottle Label)

Label for Medrol 4 mg methylprednisolone tablets, USP, featuring Pfizer branding. The label indicates a package of 100 tablets, Rx only, with storage instructions to keep at controlled room temperature 20° to 25°C and protection from light. It includes dispensing and dosage advice, with distribution by Pharmacia & Upjohn Co., a Pfizer division.*

FDA Label Image

Principal Display Panel (4 mg Tablet Dose Pack)

Label of Medrol Dosepak 4 mg methylprednisolone tablets, USP. The label includes a 6-day dosing schedule with times noted as Before Breakfast, After Lunch, After Dinner, and At Bedtime. It is distributed by Pharmacia & Upjohn Co., a Division of Pfizer Inc., NY. The label includes an NDC number 0009-0056-04 and notes that the package is not child-resistant and should be kept out of reach of children.*

FDA Label Image

Principal Display Panel (4 mg Tablet Dose Pack Carton)

Packaging label for Medrol Dosepak 4 mg (methylprednisolone) tablets, USP, by Pfizer. The label specifies a blister pack containing 21 tablets. It includes storage instructions and states the product is for prescription use only. The labeler is listed as RedPharm Drug.*

FDA Label Image

Principal Display Panel (8 mg Tablet Bottle Label)

Medrol 8 mg methylprednisolone tablets label showing the Pfizer logo. The label states the product strength as 8 mg, with 25 tablets per package, and indicates Rx only status. It includes storage instructions (controlled room temperature 20° to 25°C) and advises protection from light. The label also contains barcodes, NDC number 0009-0022-01, and distributor information for Pharmacia & Upjohn Co., a division of Pfizer Inc.*

FDA Label Image

Principal Display Panel (16 mg Tablet Bottle Label)

Medrol 16 mg methylprednisolone tablets, USP packaging label showing a bottle containing 50 tablets. The label includes storage instructions to keep at controlled room temperature 20° to 25°C (68° to 77°F) and protect from light. It is marked Rx only and distributed by Pharmacia & Upjohn Co, a division of Pfizer Inc. The Pfizer logo and barcodes are shown along with NDC 0009-0073-01.*

FDA Label Image

Principal Display Panel (32 mg Bottle Tablet Label)

Label for Medrol 32 mg methylprednisolone tablets, USP, containing 25 tablets. The label includes storage instructions to keep at 20° to 25°C (68° to 77°F) and protect from light, dosage information indicating each tablet contains 32 mg of methylprednisolone, and a note for dispensing in child-resistant containers. Distributed by Pharmacia & Upjohn Co., a division of Pfizer Inc., NY, NY 10017. The label also features the Pfizer logo and relevant barcodes.*

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Label for Medrol methylprednisolone tablets, USP 2 mg by Pfizer. The label includes storage instructions, dosage and use notes, and states the package contains 100 tablets. It is Rx only and distributed by Pharmacia & Upjohn Co, a Pfizer division. The label also displays NDC and GTIN barcodes.*

* 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.