Drug Details: SECONAL SODIUM

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	SECONAL SODIUM
FDA Application No:	(NDA) 007392
Active Ingredient(s):	SECOBARBITAL SODIUM
Company:	LILLY
Original Approval or Tentative Approval Date:	July 19, 1950
Chemical Type:	2 New active ingredient
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
SECONAL SODIUM	SECOBARBITAL SODIUM	50MG/ML	INJECTABLE; INJECTION	Discontinued	No	None

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