Drug Details: HEP-LOCK

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HEP-LOCK
FDA Application No:	(NDA) 017037
Active Ingredient(s):	HEPARIN SODIUM
Company:	BAXTER HLTHCARE
Original Approval or Tentative Approval Date:	March 22, 1972
Chemical Type:	5 New manufacturer
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
HEP-LOCK	HEPARIN SODIUM	100 UNITS/ML	INJECTABLE; INJECTION	Prescription	Yes	AP
HEP-LOCK	HEPARIN SODIUM	10 UNITS/ML	INJECTABLE; INJECTION	Prescription	Yes	AP
HEP-LOCK U/P	HEPARIN SODIUM	10 UNITS/ML	INJECTABLE; INJECTION	Prescription	No	AP
HEP-LOCK U/P	HEPARIN SODIUM	100 UNITS/ML	INJECTABLE; INJECTION	Prescription	No	AP
HEPARIN SODIUM	HEPARIN SODIUM	5,000 UNITS/0.5ML	INJECTABLE; INJECTION	Prescription	No	AP
HEPARIN SODIUM	HEPARIN SODIUM	1,000 UNITS/ML	INJECTABLE; INJECTION	Prescription	No	AP
HEPARIN SODIUM	HEPARIN SODIUM	5,000 UNITS/ML	INJECTABLE; INJECTION	Prescription	No	AP
HEPARIN SODIUM	HEPARIN SODIUM	10,000 UNITS/ML	INJECTABLE; INJECTION	Prescription	No	AP

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