Home NDC 53436-252-01 NDC 53436-252-01 - VELTASSA 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 53436-252
Requested NDC 53436-252-01
Package NDCs from labels 53436-252-01, 53436-252-30
Manufacturer Vifor Pharma, Inc.
Effective date 2025-01-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type VELTASSA - Vifor Pharma, Inc. Vifor Pharma, Inc. 2025-01-31 HUMAN PRESCRIPTION DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53436-252-01 VELTASSA 1 in 1 PACKET POWDER, FOR SUSPENSION 1 23 53436-252-30 VELTASSA 30 in 1 CARTON POWDER, FOR SUSPENSION 30 23
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53436-252 VELTASSA (PATIROMER) POWDER, FOR SUSPENSION [VIFOR PHARMA, INC.] 23 Current NDC, Legacy NDC, 2 package rows 20250209_bf002984-d6c9-46df-aecb-a07733f763c1.zip
DailyMed Socrata Ingredients# openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 5 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.