FDA.reportPublic FDA data

NDC11 63323045909

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDCProduct root
63323-0459-0963323-0459
63323-0459-963323-0459
63323-459-0963323-459

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage63323-45963323-459-09DDiscontinued by firm2026-08-17

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Heparin SodiumHEPARIN SODIUMFresenius Kabi USA, LLC2a173253-dfdc-4d9d-8dee-b9c13e6fa9f52026-04-30Warnings, Adverse reactionsExact identifier
ndc (product): 63323-459
Heparin SodiumHEPARIN SODIUMFresenius Kabi USA, LLCd55b4a63-0c04-4874-b74f-9e9b9e8b008c2025-11-28Warnings, Adverse reactionsExact identifier
ndc (package): 63323-459-09
ndc (product): 63323-459
ndc11 (package): 63323045909