Home NDC 0061-4321 NDC 0061-4321 - Zuprevo 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 0061-4321
Package NDCs from labels 0061-4321-02, 0061-4321-03
Manufacturer Merck Sharp & Dohme Corp.
Effective date 2026-09-22
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0061-4321-02 Zuprevo 100 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 100 7 0061-4321-03 Zuprevo 250 mL in 1 VIAL, MULTI-DOSE INJECTION, SOLUTION 250 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0061-4321 ZUPREVO (TILDIPIROSIN) INJECTION, SOLUTION [MERCK SHARP & DOHME CORP.] 5 2 package rows 20241103_bc52d6c2-34d7-428e-8853-a4bcbe5b6310.zip
DailyMed Socrata Ingredients# Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.