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 01:59:09

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
0126-0016-61	ML - Milliliter	0126-0016	6a1ff55d-412c-4784-8b0b-2c5512f701f2	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0126-0016	0126-0016-61

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
PreviDent 5000 Dry Mouth	SODIUM FLUORIDE	Colgate Oral Pharmaceuticals, Inc.	d93ee76f-454b-40bf-9357-39a2ae3b6ccb	2026-06-10	Warnings, Adverse reactions	Exact identifier ndc (package): 0126-0016-61 ndc11 (package): 00126001661

Reported adverse events (FAERS/openFDA)#

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