FDA.reportPublic FDA data

NDC11 00406080301

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
00406-0803-0100406-0803
00406-0803-100406-0803
00406-803-0100406-803
0406-0803-010406-0803

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
Mixed Salts of a Single-Entity Amphetamine ProductDEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATESpecGx LLCe1b21fd4-8d0b-4e54-a35d-8ad84a7caa782023-10-01Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 0406-0803-01
ndc (product): 0406-0803
ndc11 (package): 00406080301

Reported adverse events (FAERS/openFDA)#

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