FDA.reportPublic FDA data

NDC11 50845024901

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 NDCProduct root
50845-0249-0150845-0249
50845-0249-150845-0249
50845-249-0150845-249

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MetalsALUMINA, AURUM METALLICUM, CARBO VEGETABILIS, CAUSTICUM, CYSTEINUM, HEPAR SUIS, HEPAR SULPHURIS CALCAREUM, NITRICUM ACIDUM, NUX VOMICA, PHYTOLACCA DECANDRA, PLATINUM METALLICUM, STANNUM METALLICUM, STILLINGIA SYLVATICA, TELLURIUM METALLICUM, X-RAYLiddell Laboratories, Inc.daa89e0d-1dd8-45eb-9f9b-0029fdcfecee2024-07-01WarningsExact identifier
ndc (package): 50845-0249-1
ndc (product): 50845-0249
ndc11 (package): 50845024901

Reported adverse events (FAERS/openFDA)#

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