NDC11 70594002309

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
70594-0023-09	70594-0023
70594-0023-9	70594-0023
70594-023-09	70594-023

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
Colistimethate	COLISTIMETHATE SODIUM	Xellia Pharmaceuticals USA LLC	8ec7dc90-825c-422e-9f4b-c8ace9d93af5	2026-03-26	Warnings, Adverse reactions	Exact identifier ndc (product): 70594-023
Colistimethate	COLISTIMETHATE SODIUM	Xellia Pharmaceuticals USA LLC	13dc3525-1879-4bd8-a922-81bc1397d5af	2024-08-29	Warnings, Adverse reactions	Exact identifier ndc (package): 70594-023-09 ndc (product): 70594-023 ndc11 (package): 70594002309

Reported adverse events (FAERS/openFDA)#

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