NDC11 00406701203

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
00406-7012-03	00406-7012
00406-7012-3	00406-7012
0406-7012-03	0406-7012

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
Buprenorphine HCl	BUPRENORPHINE HCL	SpecGx LLC	b60d514d-a88a-4fa2-a5b0-30ac29e04973	2026-06-05	Warnings, Adverse reactions	Exact identifier ndc (package): 0406-7012-03 ndc (product): 0406-7012 ndc11 (package): 00406701203

Reported adverse events (FAERS/openFDA)#

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