FDA.reportPublic FDA data

NDC 85052-101-01 - Trutakna

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
85052-101
Requested NDC
85052-101-01
Package NDCs from labels
85052-101-01, 85052-101-04
Manufacturer
Vera Therapeutics, Inc
Effective date
2026-08-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Trutakna - Vera Therapeutics, IncVera Therapeutics, Inc2026-08-05HUMAN PRESCRIPTION DRUG LABEL

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TrutaknaATACICEPTVera Therapeutics, Inc24aa29f6-ccff-45d3-89af-4d26e525cef82026-08-05Warnings, Adverse reactionsExact identifier
application number: BLA761486
ndc (package): 85052-101-01
ndc (package): 85052-101-04
ndc (product): 85052-101
ndc11 (package): 85052010101
rxcui: 2747244
rxcui: 2747237
spl id: 83f672ee-5ed8-4226-aae7-16bb625f7088
spl set id: 24aa29f6-ccff-45d3-89af-4d26e525cef8
unii: K3D9A0ICQ3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.