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 02:51:26

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
66733-958-23	ML - Milliliter	66733-958	d789986e-b9cf-47d4-a011-ea7bbe52c741	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
66733-958	66733-958-23

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLA	Proprietary name	Proper name	License type	Status	Latest source
125084	Erbitux	cetuximab	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
ERBITUX	CETUXIMAB	ImClone LLC	8bc6397e-4bd8-4d37-a007-a327e4da34d9	2026-04-16	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 66733-958-23 ndc11 (package): 66733095823

Reported adverse events (FAERS/openFDA)#

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