FDA.reportPublic FDA data

NDC11 68001036804

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
68001-0368-0468001-0368
68001-0368-468001-0368
68001-368-0468001-368

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
Duloxetine Delayed-ReleaseDULOXETINE HYDROCHLORIDEBluePoint Laboratoriesa95cc04c-58e9-487f-8992-ef30df03a3cd2024-02-14Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 68001-368-04
ndc (product): 68001-368
ndc11 (package): 68001036804