Home NDC 0074-3410 NDC 0074-3410 - Lupron Depot-PED 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 0074-3410
Package NDCs from labels 0074-3410-01
Manufacturer AbbVie Inc.
Effective date 2025-11-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Lupron Depot-PED - AbbVie Inc. AbbVie Inc. 2025-11-14 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0074-3410-01 Lupron Depot-PED 1.5 mL in 1 SYRINGE INJECTION, POWDER, LYOPHILIZED, 1.5 mL 45 mg in 1.5mL 97
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0074-3410 LUPRON DEPOT-PED (LEUPROLIDE ACETATE) KIT [ABBVIE INC.] 93 Unmatched 20241109_e99f47d2-da10-3127-ecb3-e5d942ae6e81.zip
DailyMed Socrata Ingredients#