NDC11 00406895201

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
00406-8952-01	00406-8952
00406-8952-1	00406-8952
0406-8952-01	0406-8952

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
Mixed Salts of a Single Entity Amphetamine Product XR	DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE	SpecGx LLC	60a2834c-38a2-480e-b89c-563e9cf0c9c3	2025-11-25	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0406-8952-01 ndc (product): 0406-8952 ndc11 (package): 00406895201

Reported adverse events (FAERS/openFDA)#

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