Drug Details: DELCOBESE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	DELCOBESE
FDA Application No:	(ANDA) 083564
Active Ingredient(s):	AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE
Company:	TEVA
Original Approval or Tentative Approval Date:	October 24, 1975

There are no 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
DELCOBESE	AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE	1.25MG; 1.25MG; 1.25MG; 1.25MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None
DELCOBESE	AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE	2.5MG; 2.5MG; 2.5MG; 2.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None
DELCOBESE	AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE	3.75MG; 3.75MG; 3.75MG; 3.75MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None
DELCOBESE	AMPHETAMINE ADIPATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE ADIPATE; DEXTROAMPHETAMINE SULFATE	5MG; 5MG; 5MG; 5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE; ORAL	Discontinued	No	None

Comments for DELCOBESE

Name: *

Email: *

Text:
(HTML OK)

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

There are no comments.