NDC11 70511010150

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
70511-0101-50	70511-0101
70511-101-50	70511-101

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	MAIA PHARMACEUTICALS, INC	3529be10-0004-4628-9ca1-67a8acd86b51	2023-07-05	Warnings, Adverse reactions	Exact identifier ndc (package): 70511-101-50 ndc (product): 70511-101 ndc11 (package): 70511010150

Reported adverse events (FAERS/openFDA)#

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