NDC 42546-710-05 - PruMyx

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: 42546-710
Requested NDC: 42546-710-05
Package NDCs from labels: 42546-710-05
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
PruMyx External Cream	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	Form	Quantity	Strength	SPL version
42546-710-05	PruMyx	1 in 1 BOX		1		1
42546-710-05	PruMyx	140 g in 1 TUBE		140		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
42546-710	PRUMYX () [PRUGEN, INC.]	1	2 package rows	20120829_85f80d40-40a9-4dbb-bdbf-1663d5cbb84a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
42546-710-05	GM - Gram	42546-710	36e1bc86-6ca7-4602-bac2-6de60d33de1c	1	2013-02-19

Reported adverse events (FAERS/openFDA)#

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