Drug Details: K+10

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	K+10
FDA Application No:	(ANDA) 070999
Active Ingredient(s):	POTASSIUM CHLORIDE
Company:	ALRA
Original Approval or Tentative Approval Date:	October 22, 1987

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
K+10	POTASSIUM CHLORIDE	10MEQ	TABLET, EXTENDED RELEASE; ORAL	Prescription	No	BC

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