NDC11 59469030350

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
59469-0303-50	59469-0303
59469-303-50	59469-303

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
BRONCHI-PERTU	BRYONIA DIOICA ROOT, PROTORTONIA CACTI, GUAIACUM OFFICINALE RESIN, OENANTHE AQUATICA FRUIT, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, USNEA BARBATA, AND GRINDELIA HIRSUTULA WHOLE	PEKANA Naturheilmittel GmbH	6812a35d-4f1b-45c2-a893-a345924af03f	2022-12-23	Warnings	Exact identifier ndc (package): 59469-303-50 ndc (product): 59469-303 ndc11 (package): 59469030350

Reported adverse events (FAERS/openFDA)#

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