NDC 0009-0477 - Tolinase

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: 0009-0477
Package NDCs from labels: 0009-0477-06
Manufacturer: Pharmacia and Upjohn Company
Effective date: 2006-04-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Tolinase - Pharmacia and Upjohn Company	Pharmacia and Upjohn Company	2006-04-11	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0009-0477-06	Tolinase	100 in 1 BOTTLE, UNIT-DOSE	TABLET	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0009-0477	TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1	1 package rows	20060412_AAE8B7A4-742A-4BEC-A283-31B9408EE1AA.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
tolazamide	ACTIVE INGREDIENT	9LT1BRO48Q	TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1
tolazamide	ACTIVE MOIETY	9LT1BRO48Q	TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1
calcium sulfate	INACTIVE INGREDIENT	E934B3V59H	TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1
docusate sodium	INACTIVE INGREDIENT	F05Q2T2JA0	TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1
methylcellulose	INACTIVE INGREDIENT		TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	1
sodium alginate	INACTIVE INGREDIENT		TOLINASE (TOLAZAMIDE) TABLET [PHARMACIA AND UPJOHN COMPANY]	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
31A1819D-DA81-295F-DEB9-4D26AED30346			AAE8B7A4-742A-4BEC-A283-31B9408EE1AA	2006-04-11	Warnings, Adverse reactions	Exact identifier spl id: 31A1819D-DA81-295F-DEB9-4D26AED30346 spl set id: AAE8B7A4-742A-4BEC-A283-31B9408EE1AA

Reported adverse events (FAERS/openFDA)#

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