FDA.reportPublic FDA data

NDC 87755-0003-01 - Spirudio

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
87755-0003
Requested NDC
87755-0003-01
Package NDCs from labels
87755-0003-1, 87755-0003-01
Manufacturer
Progressive Health Research LLC
Effective date
2026-06-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Spirudio - Progressive Health Research LLCProgressive Health Research LLC2026-06-08HUMAN OTC DRUG LABEL

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 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SpirudioSPIRUDIOProgressive Health Research LLC53c3bad0-ba11-c726-e063-6394a90a64822026-06-08WarningsExact identifier
ndc (package): 87755-0001-1
ndc (package): 87755-0003-1
ndc (package): 87755-0002-1
ndc (product): 87755-0002
ndc (product): 87755-0003
ndc (product): 87755-0001
ndc11 (package): 87755000301
spl id: 53c3bb7b-3259-e3c1-e063-6394a90a4c98
spl set id: 53c3bad0-ba11-c726-e063-6394a90a6482
unii: A4FH976KAQ
SpirudioSPIRUDIOPROGRESYVUS TYRIMAI MB537294e5-3646-7e41-e063-6294a90a145a2026-06-04WarningsExact identifier
ndc (product): 87754-0001
ndc (product): 87754-0003
ndc (product): 87754-0002
spl id: 537294e5-3647-7e41-e063-6294a90a145a
spl set id: 537294e5-3646-7e41-e063-6294a90a145a
unii: A4FH976KAQ
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U

Reported adverse events (FAERS/openFDA)#

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