NDC11 81665020301

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
81665-0203-01	81665-0203
81665-0203-1	81665-0203
81665-203-01	81665-203

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 PHENYLACETATE and SODIUM BENZOATE	SODIUM PHENYLACETATE AND SODIUM BENZOATE	Omnivium Pharmaceuticals LLC	9067c301-74f9-457a-9b0f-b7e9b06a3508	2025-02-15	Warnings, Adverse reactions	Exact identifier ndc (package): 81665-203-01 ndc (product): 81665-203 ndc11 (package): 81665020301

Reported adverse events (FAERS/openFDA)#

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