NDC11 63479180901

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
63479-1809-0163479-1809
63479-1809-163479-1809

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
R09 SPLEENADENOSINE TRIPHOSPHATE, BAPTISIA TINCTORIA ROOT, CEANOTHUS AMERICANUS LEAF, FUCUS VESICULOSUS, PODOPHYLLUM RESIN, SEPIA OFFICINALIS JUICE, TESTOSTERONEApex Energetics Inc.bb8b301d-0048-16bd-e053-2a95a90a045a2024-01-08WarningsExact identifier
ndc (package): 63479-1809-1
ndc (product): 63479-1809
ndc11 (package): 63479180901

Reported adverse events (FAERS/openFDA)#

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