Drug Details: HUMULIN BR

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HUMULIN BR
FDA Application No:	(NDA) 019529
Active Ingredient(s):	INSULIN RECOMBINANT HUMAN
Company:	LILLY
Original Approval or Tentative Approval Date:	April 28, 1986
Chemical Type:	3 New dosage form
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
HUMULIN BR	INSULIN RECOMBINANT HUMAN	100 UNITS/ML	INJECTABLE; INJECTION	Discontinued	No	None

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