FDA.reportPublic FDA data

NDC 72606-051-06 - Tocilizumab-anoh

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
72606-051
Requested NDC
72606-051-06
Package NDCs from labels
72606-051-01, 72606-051-02, 72606-051-03, 72606-051-04, 72606-051-05, 72606-051-06
Manufacturer
CELLTRION USA, Inc.
Effective date
2026-01-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tocilizumab-anoh - CELLTRION USA, Inc.CELLTRION USA, Inc.2026-01-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72606-051-01Tocilizumab-anoh0.9 mL in 1 SYRINGE, GLASSINJECTION, SOLUTION, CONCENTRATE0.94
72606-051-01Tocilizumab-anoh1 in 1 CARTONINJECTION, SOLUTION, CONCENTRATE14
72606-051-02Tocilizumab-anoh0.9 mL in 1 SYRINGE, GLASSINJECTION, SOLUTION, CONCENTRATE0.94
72606-051-02Tocilizumab-anoh4 in 1 CARTONINJECTION, SOLUTION, CONCENTRATE44
72606-051-03Tocilizumab-anoh12 in 1 CARTONINJECTION, SOLUTION, CONCENTRATE124
72606-051-03Tocilizumab-anoh0.9 mL in 1 SYRINGE, GLASSINJECTION, SOLUTION, CONCENTRATE0.94
72606-051-04Tocilizumab-anoh0.9 mL in 1 SYRINGE, GLASSINJECTION, SOLUTION, CONCENTRATE0.94
72606-051-04Tocilizumab-anoh1 in 1 CARTONINJECTION, SOLUTION, CONCENTRATE14
72606-051-05Tocilizumab-anoh4 in 1 CARTONINJECTION, SOLUTION, CONCENTRATE44
72606-051-05Tocilizumab-anoh0.9 mL in 1 SYRINGE, GLASSINJECTION, SOLUTION, CONCENTRATE0.94
72606-051-06Tocilizumab-anoh12 in 1 CARTONINJECTION, SOLUTION, CONCENTRATE124
72606-051-06Tocilizumab-anoh0.9 mL in 1 SYRINGE, GLASSINJECTION, SOLUTION, CONCENTRATE0.94

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72606-051TOCILIZUMAB-ANOH (TOCILIZUMAB) INJECTION, SOLUTION, CONCENTRATE [CELLTRION USA, INC.]212 package rows20250302_60381a7e-d7ae-4384-925d-c19c418d1663.zip

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 8 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TYENNETOCILIZUMAB-AAZGFresenius Kabi USA, LLCad76441d-da59-47df-8d9d-2243005180f02026-08-26Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I031V2H011
AVTOZMATOCILIZUMABCELLTRION USA, Inc.581c288f-8015-40ef-a4c3-683c96db193d2026-07-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2705425
rxcui: 2705443
rxcui: 2705450
rxcui: 2705435
rxcui: 2705452
unii: I031V2H011
TYENNETOCILIZUMAB-AAZGFresenius Kabi USA, LLC87ac5047-4f2b-4571-a8a8-32e08865f3792026-07-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I031V2H011
TOFIDENCETOCILIZUMABOrganon LLC1ab3207a-ebfe-4565-9ce5-3a1538815c832026-05-22Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I031V2H011
TYENNETOCILIZUMAB-AAZGFresenius Kabi USA, LLCe400bbe6-43c5-4de6-82b9-cb44ce3cd9062026-05-15Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I031V2H011
bacf86b8-9d2f-45d2-9c35-4f619ea494aa60381a7e-d7ae-4384-925d-c19c418d16632026-01-23Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: bacf86b8-9d2f-45d2-9c35-4f619ea494aa
spl set id: 60381a7e-d7ae-4384-925d-c19c418d1663
TofidenceTOCILIZUMABBiogen MA Inc00529b23-850a-42b9-a152-125a95b5242c2025-12-19Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I031V2H011
ACTEMRATOCILIZUMABGenentech, Inc.2e5365ff-cb2a-4b16-b2c7-e35c6bf2de132025-12-16Boxed warning, Warnings, Adverse reactionsExact identifier
unii: I031V2H011

Reported adverse events (FAERS/openFDA)#

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