NDC11 00409329461

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
00409-3294-61	00409-3294
0409-3294-61	0409-3294

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
Potassium Acetate	POTASSIUM ACETATE	Hospira, Inc.	c58f8112-d587-493a-91b7-2b48c80bb7bf	2026-04-27	Warnings, Adverse reactions	Exact identifier ndc (product): 0409-3294
Potassium Acetate	POTASSIUM ACETATE	Hospira, Inc.	e9772b82-1e2b-4c4b-aa47-677491dbf73c	2026-04-27	Warnings, Adverse reactions	Exact identifier ndc (package): 0409-3294-61 ndc (product): 0409-3294 ndc11 (package): 00409329461

Reported adverse events (FAERS/openFDA)#

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