FDA.reportPublic FDA data

NDC 0009-0291 - Heparin Sodium

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
0009-0291
Package NDCs from labels
0009-0291-01
Effective date
2006-04-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Heparin Sodium Injection, USP2006-04-13HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0009-0291-01Heparin Sodium10 mL in 1 VIALINJECTION, SOLUTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0009-0291HEPARIN SODIUM (HEPARIN SODIUM) INJECTION, SOLUTION [PHARMACIA & UPJOHN COMPANY]11 package rows20071212_EFCDB321-832B-4554-8049-DBBB33B48334.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Heparin SodiumACTIVE INGREDIENTZZ45AB24CAHEPARIN SODIUM (HEPARIN SODIUM) INJECTION, SOLUTION1
HeparinACTIVE MOIETYT2410KM04AHEPARIN SODIUM (HEPARIN SODIUM) INJECTION, SOLUTION1
benzyl alcoholINACTIVE INGREDIENTLKG8494WBHHEPARIN SODIUM (HEPARIN SODIUM) INJECTION, SOLUTION1
sodium chlorideINACTIVE INGREDIENT451W47IQ8XHEPARIN SODIUM (HEPARIN SODIUM) INJECTION, SOLUTION1

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 2 of 2 · 28 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Heparin SodiumHEPARIN SODIUMNorthstar Rx LLC2edf6d35-5cf3-b7ff-e063-6394a90a4f332025-02-19Warnings, Adverse reactionsExact identifier
rxcui: 1361226
rxcui: 1362831
rxcui: 1361615
Heparin SodiumHEPARIN SODIUMSandoz Inc.1c634e53-44d6-cdcd-e063-6294a90a92e92025-02-19Warnings, Adverse reactionsExact identifier
rxcui: 1361226
rxcui: 1362831
rxcui: 1361615
Heparin SodiumHEPARIN SODIUMMcKesson Corporation dba SKY Packaging7f05762a-7527-4796-b21e-68277aec379e2025-01-21Warnings, Adverse reactionsExact identifier
rxcui: 1361226
rxcui: 1362831
rxcui: 1361615
HEPARIN SODIUMHEPARIN SODIUMHF Acquisition Co LLC, DBA HealthFirst9bd0f982-30f4-4e38-e053-2a95a90a3e152025-01-08Warnings, Adverse reactionsExact identifier
rxcui: 1362831
Heparin SodiumHEPARIN SODIUMPhlow Corporationcece935c-1c0a-4949-b023-d6df3d53fbfa2024-05-16Warnings, Adverse reactionsExact identifier
rxcui: 1361226
HEPARIN SODIUMHEPARIN SODIUMHF Acquisition Co LLC, DBA HealthFirst971505d4-f78c-6f5d-e053-2995a90a00e02024-01-29Warnings, Adverse reactionsExact identifier
rxcui: 1362831
Heparin SodiumHEPARIN SODIUMFresenius Kabi USA, LLCa120bdfd-21e1-4024-82a7-13cfeed290c12024-01-05Warnings, Adverse reactionsExact identifier
rxcui: 1361226
Heparin SodiumHEPARIN SODIUMFresenius Kabi USA, LLC3facd525-b9ad-46d0-b63e-f13a5f6d591d2021-09-01Warnings, Adverse reactionsExact identifier
rxcui: 1361615

Reported adverse events (FAERS/openFDA)#

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