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 01:22:59

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
55513-710-01	ML - Milliliter	55513-710	2688daa4-5912-4be3-994c-4e6008f68c39	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55513-710	55513-710-01

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLA	Proprietary name	Proper name	License type	Status	Latest source
125320	Prolia	denosumab	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
Prolia	DENOSUMAB	Amgen, Inc	49e5afe9-a0c7-40c4-af9f-f287a80c5c88	2026-06-26	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 55513-710-01 ndc11 (package): 55513071001

Reported adverse events (FAERS/openFDA)#

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