NDC11 50845025201

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
50845-0252-0150845-0252
50845-0252-150845-0252
50845-252-0150845-252

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
Party DetoxAGARICUS MUSCARIUS, AVENA SATIVA, BRYONIA, CARBO ANIMALIS, CARDUUS MARIANUS, CHELIDONIUM MAJUS, CINCHONA OFFICINALIS, HEPAR SUIS, KALI IODATUM, LAPIS ALBUS, NUX VOMICA, TARAXACUM OFFICINALE, THUJA OCCIDENTALISLiddell Laboratories, Inc.661646bf-acc1-4696-8a8e-2c9da38b4baa2024-11-04WarningsExact identifier
ndc (package): 50845-0252-1
ndc (product): 50845-0252
ndc11 (package): 50845025201

Reported adverse events (FAERS/openFDA)#

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