NDC11 70069008101

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
70069-0081-01	70069-0081
70069-0081-1	70069-0081
70069-081-01	70069-081

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
Moxifloxacin Hydrochloride	MOXIFLOXACIN HYDROCHLORIDE	Somerset Therapeutics, LLC	f7c68d49-8c61-4bde-a880-4d78568e5aa0	2024-11-25	Warnings, Adverse reactions	Exact identifier ndc (package): 70069-081-01 ndc (product): 70069-081 ndc11 (package): 70069008101

Reported adverse events (FAERS/openFDA)#

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