NDC11 50268014415

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
50268-0144-15	50268-0144
50268-144-15	50268-144

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 and Naloxone HCl	BUPRENORPHINE AND NALOXONE	AvPAK	b955054b-b37d-4079-4fed-5939b763ecb4	2026-01-08	Warnings, Adverse reactions	Exact identifier ndc (package): 50268-144-15 ndc (product): 50268-144 ndc11 (package): 50268014415

Reported adverse events (FAERS/openFDA)#

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