Home NDC 72843-590 NDC 72843-590 - leuprolide acetate This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 72843-590
Package NDCs from labels 72843-590-01
Manufacturer UBI Pharma Inc.
Effective date 2026-03-29
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72843-590-01 leuprolide acetate 1 in 1 CARTON INJECTION, SOLUTION 5 mg in 1mL 6 72843-590-01 leuprolide acetate 2.8 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 2.8 mL 5 mg in 1mL 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72843-590 LEUPROLIDE ACETATE KIT [UBI PHARMA INC.] 2 Unmatched 20241027_cd46628f-055f-4da9-8c38-fa69af34eb4d.zip