NDC11 47781035803

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
47781-0358-03	47781-0358
47781-0358-3	47781-0358
47781-358-03	47781-358

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 and Naloxone Sublingual Film	BUPRENORPHINE AND NALOXONE	Alvogen Inc.	4210afeb-474c-d842-d68e-af7e0021851a	2026-01-01	Warnings, Adverse reactions	Exact identifier ndc (package): 47781-358-03 ndc (product): 47781-358 ndc11 (package): 47781035803

Reported adverse events (FAERS/openFDA)#

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