FDA.reportPublic FDA data

NDC11 71742000201

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
71742-0002-0171742-0002
71742-0002-171742-0002
71742-002-0171742-002

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
Arthri-Joint T008APIS MELLIFICA, BRYONIA (ALBA), CAUSTICUM, COLCHICUM AUTUMNALE, KALI CARBONICUM, KALMIA LATIFOLIA, LEDUM PALUSTRE, PULSATILLA (VULGARIS), RHODODENDRON CHRYSANTHUM, RHUS TOXGuangzhou Renuma Medical Systems Co., Ltd3e8e3b3b-498e-4c4a-a096-c06dd8ac3a662017-10-23WarningsExact identifier
ndc (package): 71742-0002-1
ndc (product): 71742-0002
ndc11 (package): 71742000201

Reported adverse events (FAERS/openFDA)#

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