FDA.reportPublic FDA data

National Council for Prescription Drug Programs indexing - billing unit

Manufacturer
National Council for Prescription Drug Programs
Effective date
2013-05-02
Label type
Indexing - Billing Unit
Version
1
Source
full-release
Hydrated at
2026-06-05 04:07:53

Label at a glance#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0169-7201-01EA - Each0169-72019d666b22-e742-4e8d-9c4a-89dfca5de2a912013-05-02

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0169-72010169-7201-01

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
103665Novoseven, Novoseven RtCoagulation Factor VIIa (Recombinant)351(a)Disc2026-09-01

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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