NDC 53014-847-71 - Mykrox Tablets

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: 53014-847
Requested NDC: 53014-847-71
Package NDCs from labels: 53014-847-71
Manufacturer: Celltech Pharmaceuticals, Inc.
Effective date: 2006-01-12
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Mykrox® Tablets (metolazone tablets, USP)	Celltech Pharmaceuticals, Inc.	2006-01-12	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53014-847-71	Mykrox Tablets	100 in BOTTLE, PLASTIC	TABLET	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53014-847	MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1	1 package rows	20060131_dffb4544-0e47-40cd-9baa-d622075838cc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
metolazone	ACTIVE INGREDIENT	TZ7V40X7VX	MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1
metolazone	ACTIVE MOIETY	TZ7V40X7VX	MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1
dibasic calcium phosphate	INACTIVE INGREDIENT		MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1
magnesium stearate	INACTIVE INGREDIENT		MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1
microcrystalline cellulose	INACTIVE INGREDIENT		MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1
pregelatinized starch	INACTIVE INGREDIENT		MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1
sodium starch glycolate	INACTIVE INGREDIENT		MYKROX TABLETS (METOLAZONE TABLETS) TABLET [CELLTECH PHARMACEUTICALS, INC.]	1

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
dffb4544-0e47-40cd-9baa-d622075838cc			dffb4544-0e47-40cd-9baa-d622075838cc	2006-01-12	Warnings, Adverse reactions	Exact identifier spl id: dffb4544-0e47-40cd-9baa-d622075838cc spl set id: dffb4544-0e47-40cd-9baa-d622075838cc

Reported adverse events (FAERS/openFDA)#

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