NDC11 51267089007

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
51267-0890-07	51267-0890
51267-0890-7	51267-0890
51267-890-07	51267-890

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
Contrave Extended-Release	NALTREXONE HYDROCHLORIDE AND BUPROPION HYDROCHLORIDE	Nalpropion Pharmaceuticals LLC	485ff360-32c8-11df-928b-0002a5d5c51b	2025-11-10	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 51267-890-07 ndc (product): 51267-890 ndc11 (package): 51267089007

Reported adverse events (FAERS/openFDA)#

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