NDC 72843-592 - 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
72843-592
Manufacturer
UBI Pharma Inc.
Effective date
2026-03-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Leuprolide Acetate Injection (leuprolide acetate) Rx onlyUBI Pharma Inc.2026-03-29HUMAN PRESCRIPTION DRUG LABEL