Drug Details: HEPARIN SODIUM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HEPARIN SODIUM
FDA Application No:	(NDA) 017979
Active Ingredient(s):	HEPARIN SODIUM
Company:	ABRAXIS PHARM
Original Approval or Tentative Approval Date:	December 21, 1978
Chemical Type:	5 New manufacturer
Review Classification:	S Standard review drug

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
HEPARIN SODIUM	HEPARIN SODIUM	1,000 UNITS/ML	INJECTABLE; INJECTION	Discontinued	No	None
HEPARIN SODIUM	HEPARIN SODIUM	10,000 UNITS/ML	INJECTABLE; INJECTION	Discontinued	No	None
HEPARIN SODIUM	HEPARIN SODIUM	5,000 UNITS/ML	INJECTABLE; INJECTION	Discontinued	No	None

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