Drug Details: RUBIVITE

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	RUBIVITE
FDA Application No:	(NDA) 010791
Active Ingredient(s):	CYANOCOBALAMIN
Company:	BEL MAR
Original Approval or Tentative Approval Date:	July 14, 1958
Chemical Type:	5 New manufacturer
Review Classification:	S Standard review drug

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
RUBIVITE	CYANOCOBALAMIN	0.05MG/ML	INJECTABLE; INJECTION	Discontinued	No	None
RUBIVITE	CYANOCOBALAMIN	0.1MG/ML	INJECTABLE; INJECTION	Discontinued	No	None
RUBIVITE	CYANOCOBALAMIN	1MG/ML	INJECTABLE; INJECTION	Discontinued	No	None
RUBIVITE	CYANOCOBALAMIN	0.03MG/ML	INJECTABLE; INJECTION	Discontinued	No	None
RUBIVITE	CYANOCOBALAMIN	0.12MG/ML	INJECTABLE; INJECTION	Discontinued	No	None

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