FDA.reportPublic FDA data

AVONEX

Product NDC
59627-111
11-digit product format
596270111
Labeler code
59627
Product ID
59627-111_ab554941-0dbb-4416-981d-10bf8f8a136c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
interferon beta-1a
Dosage form
KIT
Route
INTRAMUSCULAR
Labeler
Biogen Inc.
Application
BLA103628
Marketing category
BLA
Marketing start
2014-08-29
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Reported adverse events (FAERS/openFDA)#

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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59627-111-03EA - Each59627-111e8ed3fd0-ff87-41bf-a1eb-95ea038bc85812015-04-03

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
AvonexINTERFERON BETA-1ABiogen Inc.d70a39cc-de15-4c12-a1ec-8063b69ea0e12025-11-19Warnings, Adverse reactionsExact identifier
application number: BLA103628

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
103628Avonexinterferon beta-1a351(a)Disc2026-09-01