NDC 0023-6082-01 - INFED

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
0023-6082
Requested NDC
0023-6082-01
Package NDCs from labels
0023-6082-01, 0023-6082-10
Manufacturer
Henry Schein, Inc.
Effective date
2026-04-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
INFED - Henry Schein, Inc.Henry Schein, Inc.2026-04-15HUMAN PRESCRIPTION DRUG LABEL
IRON DEXTRAN - HF Acquisition Co LLC, DBA HealthFirstHF Acquisition Co LLC, DBA HealthFirst2025-01-08HUMAN PRESCRIPTION DRUG LABEL
INFeD - Allergan, Inc.Allergan, Inc.2024-08-02HUMAN PRESCRIPTION DRUG LABEL
INFED - General Injectables & Vaccines, Inc.General Injectables & Vaccines, Inc.2022-12-22HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0023-6082-01INFeD2 mL in 1 VIAL, SINGLE-DOSEINJECTION219
0023-6082-10INFeD10 in 1 CARTONINJECTION1019

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0023-6082INFED (IRON DEXTRAN) INJECTION [ALLERGAN, INC.]19Current NDC, Legacy NDC, 2 package rows20250511_94b01b1e-794b-4bea-8e24-2e54683fc023.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0023-6082-01ML - Milliliter0023-60827f6a9f5f-a9c4-481b-a84b-fffa2a4e789612025-05-14
0023-6082-10ML - Milliliter0023-6082a3be9fbb-d433-47b9-acdc-a5c82919457812019-02-13

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 · 6 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
INFEDIRON DEXTRANHenry Schein, Inc.99bf34be-cb8a-46d1-9637-5544dc2da2872026-04-15Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA017441
ndc (package): 0404-9879-02
ndc (product): 0404-9879
rxcui: 206216
rxcui: 311144
spl id: 6dc448fd-d581-4cdb-a4a5-818a41f60c23
spl set id: 99bf34be-cb8a-46d1-9637-5544dc2da287
unii: 95HR524N2M
Se-Tan PLUSMULTIVITAMIN/MINERALSeton Pharmaceuticals56e912df-3a49-4405-8df1-7b80d12bd9202025-04-24Boxed warning, Adverse reactionsExact identifier
unii: 95HR524N2M
IRON DEXTRANIRON DEXTRANHF Acquisition Co LLC, DBA HealthFirst9a4cd424-865d-fdd1-e053-2995a90a00ff2025-01-08Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA017441
ndc (package): 51662-1441-1
ndc (product): 51662-1441
rxcui: 311144
spl id: 2b3948f4-fdef-5321-e063-6394a90ad70c
spl set id: 9a4cd424-865d-fdd1-e053-2995a90a00ff
unii: 95HR524N2M
INFeDIRON DEXTRANAllergan, Inc.94b01b1e-794b-4bea-8e24-2e54683fc0232024-08-02Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA017441
ndc (package): 0023-6082-10
ndc (package): 0023-6082-01
ndc (product): 0023-6082
ndc11 (package): 00023608201
rxcui: 206216
rxcui: 311144
spl id: d6b2a709-570d-4ceb-8772-7961d247a42b
spl set id: 94b01b1e-794b-4bea-8e24-2e54683fc023
unii: 95HR524N2M
PureVit DualFe PlusFERROUS FUMARATE, POLYSACCHARIDE IRON COMPLEXPureTek Corporation71f63741-cad4-43b5-bb3e-c63a188d10a22023-01-11Warnings, Adverse reactionsExact identifier
unii: 95HR524N2M
dc1d131d-b3e7-4759-b61b-fd18765201d43cbcd123-0097-4778-98df-09371837c3a62022-12-22Warnings, Adverse reactionsExact identifier
spl id: dc1d131d-b3e7-4759-b61b-fd18765201d4
spl set id: 3cbcd123-0097-4778-98df-09371837c3a6

Reported adverse events (FAERS/openFDA)#

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