Drug Details: INFUMORPH

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	INFUMORPH
FDA Application No:	(NDA) 018565
Active Ingredient(s):	MORPHINE SULFATE
Company:	BAXTER HLTHCARE
Original Approval or Tentative Approval Date:	September 18, 1984
Chemical Type:	3 New dosage form
Review Classification:	P Priority review drug
	O Orphan drug

There are no 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
DURAMORPH PF	MORPHINE SULFATE	0.5MG/ML	INJECTABLE; INJECTION	Prescription	Yes	AP
DURAMORPH PF	MORPHINE SULFATE	1MG/ML	INJECTABLE; INJECTION	Prescription	Yes	AP
INFUMORPH	MORPHINE SULFATE	10MG/ML	INJECTABLE; INJECTION	Prescription	Yes	None
INFUMORPH	MORPHINE SULFATE	25MG/ML	INJECTABLE; INJECTION	Prescription	Yes	None

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