Home NDC 83831-150 NDC 83831-150 - LUTRATE DEPOT 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 83831-150
Package NDCs from labels 83831-150-22
Manufacturer Avyxa Pharma, LLC
Effective date 2025-06-03
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type LUTRATE DEPOT - Avyxa Pharma, LLC Avyxa Pharma, LLC 2025-06-03 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83831-150-22 LUTRATE DEPOT 2 mL in 1 VIAL, SINGLE-DOSE INJECTION, POWDER, LYOPHILIZED, 2 mL 22.5 mg in 2mL 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83831-150 LUTRATE DEPOT (LEUPROLIDE ACETATE) KIT [AVYXA PHARMA, LLC] 1 Unmatched 20250330_3a6d1373-17d9-4289-b62f-d299ffe55831.zip