Allopurinol Structural Formula (All0d 0001 01)
Allopurinol Injection, Powder, Lyophilized, For Solution
Product Images NDC 65219-380
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Allopurinol (NDC 65219-380). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fresenius Kabi Usa, 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.
Fresenius Kabi Logo (All0d 0001 02)
Principal Display Panel – Shelf Carton (All0d 0001 03)
This is a description of the drug Allopurinol for Injection, used in intravenous infusion, supplied in single-dose vials containing 500 mg/vial of Allopurinol. The drug has to be used within 10 hours after reconstitution by injecting 25 mL of sterile water. The solution contains 500 mg of Allopurinol and should be further diluted before intravenous administration. The usual dosage and reconstitution instructions can be found in the accompanying prescribing information. The drug should be stored at a temperature of 20°C to 25°C. The manufacturer's name is not available in the given text.*
Principal Display Panel – Vial Label (All0d 0001 04)
This is a description of Allopurinol for Injection. Each vial of this product contains 500mg of allopurinol. The solution should be prepared and then further diluted before being administered intravenously. The usual dosage and reconstitution instructions can be found in the accompanying prescribing information. The product should be stored at 20°C to 25°C and unused portions should be discarded. This product is manufactured by Fresenius Kabi in India.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
