NDC11 00904701006

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
00904-7010-06	00904-7010
00904-7010-6	00904-7010
0904-7010-06	0904-7010

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 hydrochloride and naloxone hydrochloride dihydrate	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE	Major Pharmaceuticals	c5fbec69-e7de-44a8-b9fa-0378ae61a9fe	2026-03-03	Warnings, Adverse reactions	Exact identifier ndc (package): 0904-7010-06 ndc (product): 0904-7010 ndc11 (package): 00904701006

Reported adverse events (FAERS/openFDA)#

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