NDC 42546-130-45 - PruTect

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 42546-130
Requested NDC: 42546-130-45
Package NDCs from labels: 42546-130-45, 42546-130-90
Manufacturer: PruGen, Inc.
Effective date: 2012-08-22
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PruTect Topical Emulsion	PruGen, Inc.	2012-08-22	PRESCRIPTION MEDICAL DEVICE LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2013-02-19	Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Quantity	SPL version
42546-130-45	PruTect	1 in 1 BOX	1	1
42546-130-45	PruTect	45 g in 1 TUBE	45	1
42546-130-90	PruTect	90 g in 1 TUBE	90	1
42546-130-90	PruTect	1 in 1 BOX	1	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42546-130	PRUTECT () [PRUGEN, INC.]	1	4 package rows	20120827_090ceba7-5232-48db-b96b-1ed8e43ba52f.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
42546-130-45	GM - Gram	42546-130	36c6e4ff-402e-4e94-8955-e7e0f2438f6e	1	2013-02-19
42546-130-90	GM - Gram	42546-130	6c29596b-cd7a-4b7d-92fd-50d23562befc	1	2013-02-19

Reported adverse events (FAERS/openFDA)#

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