NDC11 73317880101

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
73317-8801-01	73317-8801
73317-8801-1	73317-8801

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
AUM Alcohol Pad	ALCOHOL PAD	SLV PHARMACEUTICALS LLC DBA AUM PHARMACEUTICALS	632da1b7-70bb-467d-81b2-39536f9fff3c	2025-02-26	Warnings	Exact identifier ndc (package): 73317-8801-1 ndc (product): 73317-8801 ndc11 (package): 73317880101

Reported adverse events (FAERS/openFDA)#

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