NDC11 72189057960

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
72189-0579-60	72189-0579
72189-579-60	72189-579

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 Sublingual	BUPRENORPHINE SUBLINGUAL	Direct_rx	2204e135-6a0c-68a2-e063-6394a90ac019	2024-09-13	Warnings, Adverse reactions	Exact identifier ndc (package): 72189-579-60 ndc (product): 72189-579 ndc11 (package): 72189057960

Reported adverse events (FAERS/openFDA)#

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