NDC 0009-0023-01 - Cortisone Acetate

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: 0009-0023
Requested NDC: 0009-0023-01
Package NDCs from labels: 0009-0023-01
Manufacturer: Pharmacia and Upjohn Company
Effective date: 2006-01-04
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cortisone Acetate - Pharmacia and Upjohn Company	Pharmacia and Upjohn Company	2006-01-04	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Cortisone Acetate	ACTIVE INGREDIENT	883WKN7W8X	CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
Cortisone	ACTIVE MOIETY	V27W9254FZ	CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
calcium stearate	INACTIVE INGREDIENT	776XM7047L	CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
corn starch	INACTIVE INGREDIENT		CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
lactose	INACTIVE INGREDIENT		CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
mineral oil	INACTIVE INGREDIENT		CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
sorbic acid	INACTIVE INGREDIENT	X045WJ989B	CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2
sucrose	INACTIVE INGREDIENT	C151H8M554	CORTISONE ACETATE (CORTISONE ACETATE) TABLET [PHARMACIA AND UPJOHN COMPANY]	2

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
6044B257-9947-3160-E3D7-A96358DCF711			73673E2D-8D33-4719-92CE-AB619DE343B0	2006-01-04	Warnings, Adverse reactions	Exact identifier spl id: 6044B257-9947-3160-E3D7-A96358DCF711 spl set id: 73673E2D-8D33-4719-92CE-AB619DE343B0

Reported adverse events (FAERS/openFDA)#

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