FDA.reportPublic FDA data

NDC11 10702007006

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
10702-0070-0610702-0070
10702-0070-610702-0070
10702-070-0610702-070

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
Oxymorphone HydrochlorideOXYMORPHONE HYDROCHLORIDEKVK-Tech, Inc.dcb5b5d2-7d0a-497a-8f1e-3b96fd43320b2026-01-30Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 10702-070-06
ndc (product): 10702-070
ndc11 (package): 10702007006

Reported adverse events (FAERS/openFDA)#

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