Azathioprine Tablet
Product Images NDC 68682-231

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Azathioprine (NDC 68682-231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oceanside Pharmaceuticals, 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

Adverse Reaction Table (Adverse Reaction Table Pc5423a)

A data table presenting toxicity rates related to Azathioprine use in patients with Renal Homograft and Rheumatoid Arthritis. The table lists incidences of leukopenia (any degree and <2500 cells/mm³), infections, and neoplasia subdivided into lymphoma and others, with corresponding percentage values for each condition.*

FDA Label Image

Azathioprine Structure (Azathioprine Structure Pc5423a)

Chemical structure of Azathioprine, showing its molecular formula C9H7N7O2S and molecular weight 277.27.*

FDA Label Image

75mg Tablets (Pc5421a)

Azathioprine Tablets, USP 75 mg oral tablets from Oceanside Pharmaceuticals. The label indicates 100 tablets per package with a scored, yellow tablet. The label includes storage instructions, dosage advisory, manufacturer Alcami Corporation, and distributor Oceanside Pharmaceuticals.*

FDA Label Image

100 mg Tablets (Pc5422a)

Azathioprine Tablets, USP 100 mg oral tablets label displaying 100 tablets per bottle. The label includes dosage strength, directions to see package insert for usual dosage, storage instructions, and warnings to keep out of reach of children. Distributed by Oceanside Pharmaceuticals and manufactured by Alcami Corporation, with a barcode and NDC 68682-241-01.*

* 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.