Allopurinol
Product Images NDC 61919-748

3 FDA label images from Direct Rx · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Allopurinol (NDC 61919-748). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

471 (471 30)

471 (471 30)
ALLOPURINOL 300mg 30 Tablets packaging label from DIRECT RX. The label states it is a generic for ZYLOPRIM and that each tablet contains Allopurinol USP 300mg. The label also includes NDC 61919-471-30, lot number 471-30, and an expiration discard date of 01/19. Additional distribution and packaging information is visible.*
FDA Label Image

61919 0748 30

61919 0748 30
ALLOPURINOL 100 mg tablet label for 30 tablets. The label indicates it is generic for ZYLOPRIM and each tablet contains Allopurinol USP 100 mg. Packaged and distributed by DIRECT Rx, with a sample lot and discard date of 11/30/21. The label includes NDC code 61919-748-30 and manufacturing information from Accord Healthcare Inc.*
FDA Label Image

61919 0748 90

61919 0748 90
ALLOPURINOL 100 mg tablets, packaged in a bottle containing 90 tablets, labeled as a generic for ZYLOPRIM. The label shows the dosage strength, tablet count, and manufacturer details including Direct Rx as the packager and distributor. Additional information includes sample lot and expiration date of 12/31/22.*

* 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.