Home NDC 0781-3006 NDC 0781-3006 - 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 0781-3006
Package NDCs from labels 0781-3006-42
Manufacturer Sandoz Inc
Effective date 2026-05-19
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Leuprolide Acetate - Sandoz Inc Sandoz Inc 2026-05-19 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0781-3006-42 Leuprolide Acetate 2.8 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 2.8 mL 1 mg in 0.2mL 24 0781-3006-42 Leuprolide Acetate 1 in 1 CARTON INJECTION, SOLUTION 1 mg in 0.2mL 24
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0781-3006 LEUPROLIDE ACETATE KIT [BRYANT RANCH PREPACK] 101 Unmatched 20220428_19afe51a-3b2d-4286-ad32-992a34bba648.zip 0781-3006 LEUPROLIDE ACETATE KIT [SANDOZ INC] 21 Unmatched 20241204_8bd72c1e-2751-4498-a346-bc5e3acbba0b.zip
DailyMed Socrata Ingredients#