Drug Details: DELTA-CORTEF

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	DELTA-CORTEF
FDA Application No:	(NDA) 009987
Active Ingredient(s):	PREDNISOLONE
Company:	PHARMACIA AND UPJOHN
Original Approval or Tentative Approval Date:	June 21, 1955
Chemical Type:	1 New molecular entity (NME)
Review Classification:	S Standard review drug

Therapeutic Equivalents	Labels are not available
Approval History, Letters, Reviews and Related Documents

You can see the products in the same application. The table can be sorted by clicking the header columns.

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code
DELTA-CORTEF	PREDNISOLONE	5MG	TABLET; ORAL	Discontinued	No	None

Comments for DELTA-CORTEF

Name: *

Email: *

Text:
(HTML OK)

Enter the code from the picture: *
(click here to load another image)

There are no comments.