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 02:42:17

Label at a glance#

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1102207	IROSPAN 24/6 KIT (Pack)	{6 (ascorbic acid 100 MG / biotin 0.3 MG / calcium carbonate 100 MG / calcium pantothenate 7 MG / folic acid 1 MG / niacin 25 MG / pyridoxine hydrochloride 30 MG / riboflavin 5 MG / succinic acid 150 MG / thiamine hydrochloride 5 MG / vitamin B12 0.01 MG Oral Tablet) / 24 (ascorbic acid 100 MG / biotin 0.3 MG / calcium pantothenate 0.3 MG / ferrous bisglycinate 65 MG / folic acid 1 MG / formic acid 155 MG / iron-dextran complex 65 MG / niacin 25 MG / pyridoxine hydrochloride 30 MG / riboflavin 5 MG / thiamine hydrochloride 5 MG / vitamin B12 0.01 MG Oral Tablet [Irospan Tablet]) } Pack [Irospan 24/6 Kit]	BPCK Active

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
50967-126-30	EA - Each	50967-126	ce4cd851-65f6-42d8-8c73-c7f99ea3c2aa	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50967-126	50967-126-30

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
IROSPAN 24/6	IRON, FOLIC ACID, VITAMIN/MINERAL SUPPLEMENT	WOMENS CHOICE PHARMACEUTICALS LLC	0722734e-5a30-47af-99a3-2512848b45cd	2025-05-13	Boxed warning, Adverse reactions	Exact identifier ndc (package): 50967-126-30 ndc11 (package): 50967012630

Reported adverse events (FAERS/openFDA)#

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