National Council for Prescription Drug Programs indexing - billing unit

Manufacturer: National Council for Prescription Drug Programs
Effective date: 2012-07-24
Label type: Indexing - Billing Unit
Version: 1
Source: full-release
Hydrated at: 2026-06-05 02:41:51

Label at a glance#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
25682-001-01	ML - Milliliter	25682-001	cd45d664-e7f7-416b-aded-9ef2782c047b	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
25682-001	25682-001-01

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLA	Proprietary name	Proper name	License type	Status	Latest source
125166	Soliris	eculizumab	351(a)	Rx	2026-09-01

Source Document#

Source XML

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SOLIRIS	ECULIZUMAB	Alexion Pharmaceuticals Inc.	ebcd67fa-b4d1-4a22-b33d-ee8bf6b9c722	2026-07-08	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 25682-001-01 ndc11 (package): 25682000101

Reported adverse events (FAERS/openFDA)#

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