FDA.reportPublic FDA data

NDC 72603-201 - 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
72603-201
Package NDCs from labels
72603-201-01
Manufacturer
NorthStar RxLLC | RK Pharma INC
Effective date
2025-06-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Leuprolide Acetate - NorthStar RxLLC | RK Pharma INCNorthStar RxLLC | RK Pharma INC2025-06-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72603-201-01Leuprolide Acetate2.8 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION2.8 mL5 mg in 1mL7
72603-201-01Leuprolide Acetate1 in 1 CARTONINJECTION, SOLUTION5 mg in 1mL7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72603-201LEUPROLIDE ACETATE KIT [NORTHSTAR RXLLC]5Unmatched20240622_0cf31b40-816b-d055-e063-6294a90af5d0.zip