NDC11 54092038101

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 NDC	Product root
54092-0381-01	54092-0381
54092-0381-1	54092-0381
54092-381-01	54092-381

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Adderall XR	DEXTROAMPHETAMINE SULFATE, DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE SULFATE AND AMPHETAMINE ASPARTATE	Takeda Pharmaceuticals America, Inc.	aff45863-ffe1-4d4f-8acf-c7081512a6c0	2026-04-30	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 54092-381-01 ndc (product): 54092-381 ndc11 (package): 54092038101

Reported adverse events (FAERS/openFDA)#

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