Product Images Allopurinol
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Product Label Images
The following 3 images provide visual information about the product associated with Allopurinol NDC 51655-782 by Northwind Pharmaceuticals, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
Label - 51655 782 52 Master Bottle Label Approval Rev A 08 21
This is a description for Allopurinol Tablets USP, 300mg that comes in a pack of 30 tablets, which requires a prescription to use. Users are advised to read the package insert for the dosage information. The tablets are manufactured and repackaged by Dr. Reddy's Laboratories Louisiana LLC and Northwind Pharmaceuticals, respectively. The tablets with NDC number 51655-782-52 contain Allopurinol, USP as the active ingredient. These should be stored between 15° to 30°C and kept in the original container while protecting them from moisture, in a controlled room temperature. The Global Trade Item Number is 0035165782521 while the Serial Number is 000000000000000. The expiration date and the batch number of the tablets are 00/00/0000 and 0000000000, respectively.*
structure - structure
structure2 - structure2
This text is about chemical compounds related to Allopurinol and Oxipurinol, which are commonly used to treat gout and kidney stones. The text includes the chemical structures of these compounds along with their respective molecular formulas and names, as well as some related chemical compounds such as Xanthine and Uric Acid.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.