NDC11 51662155803

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
51662-1558-03	51662-1558
51662-1558-3	51662-1558

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
PROCHLORPERAZINE EDISYLATE	PROCHLORPERAZINE EDISYLATE	HF Acquisition Co LLC, DBA HealthFirst	e181c18d-32a8-587e-e053-2995a90acc5b	2024-01-30	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 51662-1558-3 ndc (product): 51662-1558 ndc11 (package): 51662155803

Reported adverse events (FAERS/openFDA)#

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