NDC11 00409018125

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
00409-0181-25	00409-0181
00409-181-25	00409-181
0409-0181-25	0409-0181

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
Gemcitabine	GEMCITABINE	Hospira, Inc.	dc02a23b-3ff9-4441-aa91-8e9e629a7315	2026-04-27	Warnings, Adverse reactions	Exact identifier ndc (product): 0409-0181
Gemcitabine	GEMCITABINE	Hospira, Inc.	e18ed1cb-7dd0-4001-bfda-17d1f4587fb8	2026-04-27	Warnings, Adverse reactions	Exact identifier ndc (package): 0409-0181-25 ndc (product): 0409-0181 ndc11 (package): 00409018125

Reported adverse events (FAERS/openFDA)#

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