fibrinogen, human 171 MG / thrombin, human 62.2 UNT Medicated Patch [TachoSil]

RxCUI
1014305
RxNorm name
fibrinogen, human 171 MG / thrombin, human 62.2 UNT Medicated Patch [TachoSil]
Display name
fibrinogen, human 171 MG / thrombin, human 62.2 UNT Medicated Patch [TachoSil]
Full name
fibrinogen, human 171 MG / thrombin, human 62.2 UNT Medicated Patch [TachoSil]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:47

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
125351TachosilFibrin Sealant Patch351(a)Rx2026-08-01

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TachoSilTHROMBIN HUMAN AND FIBRINOGENCorza Medical GmbH0c324332-290f-413f-820c-8c9a971a27662025-10-08Warnings, Adverse reactionsExact identifier
rxcui: 1014305

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
0c324332-290f-413f-820c-8c9a971a2766TachoSil 1.9 inch x 1.9 inch Patch [PSN] · fibrinogen, human 171 MG / thrombin, human 62.2 UNT Medicated Patch [TachoSil] [SBD] · TachoSil (fibrinogen, human 170.5 MG / thrombin, human 62.2 UNT) Medicated Patch [SY]37These highlights do not include all the information needed to use TACHOSIL safely and effectively. See full prescribing information for TACHOSIL. TACHOSIL ® Fibrin Sealant Patch Absorbable Patch for Topical Use Initial U.S. Approval: 201020251008