Home NDC 70510-2323 NDC 70510-2323 - RADICAVA 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 70510-2323
Package NDCs from labels 70510-2323-1
Manufacturer Shionogi Inc.
Effective date 2026-05-05
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type RADICAVA - Shionogi Inc. Shionogi Inc. 2026-05-05 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70510-2323-1 RADICAVA ORS 1 in 1 KIT SUSPENSION 735 mg in 35mL 29 70510-2323-1 RADICAVA ORS 35 mL in 1 BOTTLE SUSPENSION 1 mL 735 mg in 35mL 29
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70510-2323 RADICAVA (EDARAVONE) INJECTION RADICAVA ORS (EDARAVONE) KIT [MITSUBISHI TANABE PHARMA AMERICA, INC.] 24 Unmatched 20250305_0ce2c1c4-2a40-485c-b7cb-96a9b85d9d11.zip