Drug Details: ISUPREL

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	ISUPREL
FDA Application No:	(NDA) 010515
Active Ingredient(s):	ISOPROTERENOL HYDROCHLORIDE
Company:	HOSPIRA
Original Approval or Tentative Approval Date:	May 25, 1956
Chemical Type:	3 New dosage form
Review Classification:	P Priority review drug

Therapeutic Equivalents	Label Information
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
ISUPREL	ISOPROTERENOL HYDROCHLORIDE	0.2MG/ML	INJECTABLE; INJECTION	Prescription	Yes	AP

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