NDC11 57556001702

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
57556-0017-0257556-0017
57556-0017-257556-0017
57556-017-0257556-017

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
PulsatillaPULSATILLAHistorical Remediesc6790a91-d601-8c37-e053-2995a90a0a0c2025-10-07WarningsExact identifier
ndc (package): 57556-017-02
ndc (product): 57556-017
ndc11 (package): 57556001702

Reported adverse events (FAERS/openFDA)#

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