NDC 0187-0004-00 - Siliq

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
0187-0004
Requested NDC
0187-0004-00
Package NDCs from labels
0187-0004-00, 0187-0004-02, 0187-0004-03, 0187-0004-04
Manufacturer
Bausch Health US LLC | Patheon Italia S.p.A.
Effective date
2026-05-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Siliq - Bausch Health US LLC | Patheon Italia S.p.A.Bausch Health US LLC | Patheon Italia S.p.A.2026-05-28HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0187-0004-00Siliq1 in 1 SYRINGEINJECTION121
0187-0004-02Siliq2 in 1 CARTONINJECTION221
0187-0004-03Siliq2 in 1 CARTONINJECTION221
0187-0004-04Siliq1 in 1 SYRINGEINJECTION121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0187-0004SILIQ (BRODALUMAB) INJECTION [BAUSCH HEALTH US LLC]17Current NDC, Legacy NDC, 4 package rows20241109_1a550c33-456a-4833-814e-8591aea7c688.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0187-0004-00ML - Milliliter0187-0004bb07ca87-2dd1-469c-b280-f5f2c5f2992a12017-04-05
0187-0004-02ML - Milliliter0187-000499a658c1-def4-4b3e-8aa8-3532f412049812017-04-05

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
SiliqBRODALUMABBausch Health US LLC1a550c33-456a-4833-814e-8591aea7c6882026-05-28Boxed warning, Warnings, Adverse reactionsExact identifier
application number: BLA761032
ndc (package): 0187-0004-03
ndc (package): 0187-0004-00
ndc (package): 0187-0004-04
ndc (package): 0187-0004-02
ndc (product): 0187-0004
ndc11 (package): 00187000400
rxcui: 1872256
rxcui: 1872261
spl id: 5fbd9beb-42b9-4360-8363-71f8f0c5a52e
spl set id: 1a550c33-456a-4833-814e-8591aea7c688
unii: 6ZA31Y954Z

Reported adverse events (FAERS/openFDA)#

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