Home NDC 53020-255 NDC 53020-255 - DAPIPRAZOLE 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 53020-255
Package NDCs from labels 53020-255-01
Manufacturer Baradaina, LLC
Effective date 2024-01-09
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type DAPIPRAZOLE - Baradaina, LLC Baradaina, LLC 2024-01-09 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53020-255-01 DAPIPRAZOLE 5 mL in 1 VIAL POWDER, FOR SOLUTION 5 mL 25 mg in 5mL 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53020-255 DAPIPRAZOLE KIT [BARADAINA, LLC] 3 Unmatched 20240110_8b0fde24-9549-11cf-e053-2a95a90a9338.zip