NDC11 50090272000

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
50090-2720-0	50090-2720
50090-2720-00	50090-2720

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
Amlodipine and Benazepril Hydrochloride	AMLODIPINE AND BENAZEPRIL HYDROCHLORIDE	A-S Medication Solutions	55bfd9ea-b474-4863-8fae-1b720d91034c	2024-01-07	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 50090-2720-0 ndc (product): 50090-2720 ndc11 (package): 50090272000

Reported adverse events (FAERS/openFDA)#

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