Drug Details: TENUATE DOSPAN

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	TENUATE DOSPAN
FDA Application No:	(NDA) 012546
Active Ingredient(s):	DIETHYLPROPION HYDROCHLORIDE
Company:	WATSON PHARMS
Original Approval or Tentative Approval Date:	November 17, 1960
Chemical Type:	2 New active ingredient
Review Classification:	S Standard 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
TENUATE DOSPAN	DIETHYLPROPION HYDROCHLORIDE	75MG	TABLET, EXTENDED RELEASE; ORAL	Prescription	Yes	None

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