Drug Details: HUMULIN N

DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST

Drug Details

Drug Name:	HUMULIN N
FDA Application No:	(NDA) 018781
Active Ingredient(s):	INSULIN SUSP ISOPHANE RECOMBINANT HUMAN
Company:	LILLY
Original Approval or Tentative Approval Date:	October 28, 1982
Chemical Type:	3 New dosage form
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
HUMULIN N	INSULIN SUSP ISOPHANE RECOMBINANT HUMAN	100 UNITS/ML	INJECTABLE; INJECTION	OTC	Yes	None

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