NDC11 00409114102

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
00409-1141-02	00409-1141
00409-1141-2	00409-1141
0409-1141-02	0409-1141

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
SODIUM CHLORIDE	SODIUM CHLORIDE	Hospira, Inc.	af6aebad-ef03-4d19-9a40-18e5a278b812	2025-11-11	Warnings, Adverse reactions	Exact identifier ndc (package): 0409-1141-02 ndc (product): 0409-1141 ndc11 (package): 00409114102

Reported adverse events (FAERS/openFDA)#

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