NDC11 65862016390

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
65862-0163-90	65862-0163
65862-163-90	65862-163

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
QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE	Aurobindo Pharma Limited	50a58159-9572-4445-9859-b392632597da	2024-04-28	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 65862-163-90 ndc (product): 65862-163 ndc11 (package): 65862016390

Reported adverse events (FAERS/openFDA)#

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