NDC11 51662131702

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
51662-1317-02	51662-1317
51662-1317-2	51662-1317

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
6% HETASTARCH IN 0.9% SODIUM CHLORIDE	6% HETASTARCH IN 0.9% SODIUM CHLORIDE	HF Acquisition Co LLC, DBA HealthFirst	7b97c681-4514-c544-e053-2991aa0a3d78	2024-01-29	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 51662-1317-2 ndc (product): 51662-1317 ndc11 (package): 51662131702

Reported adverse events (FAERS/openFDA)#

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