NDC11 46708075790

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
46708-0757-90	46708-0757
46708-757-90	46708-757

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 Atorvastatin	AMLODIPINE AND ATORVASTATIN	Alembic Pharmaceuticals Limited	ecab983e-6ed8-4440-b7b4-7ac4bf39b26c	2025-05-23	Warnings, Adverse reactions	Exact identifier ndc (package): 46708-757-90 ndc (product): 46708-757 ndc11 (package): 46708075790

Reported adverse events (FAERS/openFDA)#

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