NDC11 72266023601

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
72266-0236-01	72266-0236
72266-0236-1	72266-0236
72266-236-01	72266-236

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	FOSUN PHARMA USA INC	cee1e9a2-bbe5-2419-e053-2a95a90ac3ef	2024-05-09	Warnings, Adverse reactions	Exact identifier ndc (package): 72266-236-01 ndc (product): 72266-236 ndc11 (package): 72266023601

Reported adverse events (FAERS/openFDA)#

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