NDC11 00409733420

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
00409-7334-20	00409-7334
0409-7334-20	0409-7334

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Hospira, Inc	365fc265-8e6c-432f-9fda-911f5f7fb451	2026-01-16	Warnings, Adverse reactions	Exact identifier ndc (product): 0409-7334
Ceftriaxone Sodium	CEFTRIAXONE SODIUM	Hospira, Inc	36c07ebf-b091-483e-b2c4-f0fc0c2b4186	2026-01-16	Warnings, Adverse reactions	Exact identifier ndc (package): 0409-7334-20 ndc (product): 0409-7334 ndc11 (package): 00409733420

Reported adverse events (FAERS/openFDA)#

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