Medrol Tablet
Product Images NDC 0009-0056

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Medrol (NDC 0009-0056). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharmacia & Upjohn Company 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

Chemical Structure (Medrol 01)

Chemical structure of the active ingredient in Medrol, showing the steroid backbone and attached functional groups characteristic of methylprednisolone.*

FDA Label Image

Logo (Medrol 02)

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Medrol 4 mg tablets label by Pharmacia & Upjohn Company LLC features the Pfizer logo, identifies the product as methylprednisolone tablets USP with a count of 100 tablets. It includes storage instructions to keep at controlled room temperature and protect from light, along with dosage information referencing accompanying prescribing information. The label shows a National Drug Code (NDC) and barcode.*

FDA Label Image

Principal Display Panel (4 mg Tablet Bottle Label)

DosePak blister card for Medrol 4 mg tablets (methylprednisolone) showing a 6-day dosing schedule with designated doses before breakfast, after lunch, after dinner, and at bedtime. The label lists Pharmacia & Upjohn Company LLC as the distributor and includes instructions for taking six tablets on Day 1 and subsequent divided doses on following days. The package is marked Rx only and contains a barcode, lot, and expiration placeholders.*

FDA Label Image

Principal Display Panel (4 mg Tablet Dose Pack)

Packaging label for Medrol Dosepak 4 mg tablets containing methylprednisolone, USP. The box is for one blister pack containing 21 tablets, labeled as Unit of Use. Distributed by Pharmacia & Upjohn Co, a division of Pfizer Inc. The label includes storage instructions, dosage information, and a notice that the package is not child-resistant. The design prominently features the Pfizer logo and dosage strength in green.*

FDA Label Image

Principal Display Panel (4 mg Tablet Dose Pack Carton)

Medrol 8 mg methylprednisolone tablets, USP label showing a 25-tablet package. Distributed by Pharmacia & Upjohn Company LLC, Division of Pfizer Inc. Storage instructions include keeping at 20-25°C (68-77°F) and protecting from light. It specifies dispensing in child-resistant containers and includes barcode and NDC 0009-0022-01.*

FDA Label Image

Principal Display Panel (8 mg Tablet Bottle Label)

Label for Medrol 16 mg methylprednisolone tablets, USP, distributed by Pharmacia & Upjohn Company LLC, a division of Pfizer Inc. The label indicates a package containing 50 tablets, with storage instructions to keep at controlled room temperature 20°C to 25°C, protected from light, and in child-resistant containers. The label includes the Pfizer logo, NDC 0009-0073-01, and a barcode.*

FDA Label Image

Principal Display Panel (16 mg Tablet Bottle Label)

Medrol 32 mg methylprednisolone tablets, USP label for a package of 25 tablets. Distributed by Pharmacia & Upjohn Company LLC, Division of Pfizer Inc., NY, NY 10017. The label includes storage instructions to store at controlled room temperature (20° to 25°C) and protect from light, with warnings to dispense in tight, child-resistant containers and keep patient under close observation of a physician.*

FDA Label Image

Principal Display Panel (32 mg Bottle Tablet Label)

Medrol 2 mg tablets label from Pharmacia & Upjohn Company LLC. The label includes the Pfizer logo, the proprietary name Medrol, the active ingredient methylprednisolone USP, strength 2 mg, and a quantity of 100 tablets. It also shows storage instructions, dispensing and dosage information notes, and barcode details.*

* 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.