DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
Home
Overview
Details
Browse by Letter:
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
0-9
Label and Approval History
Drug Name:
HUMULIN BR
FDA Application No:
(NDA) 019529
Active Ingredient(s):
INSULIN RECOMBINANT HUMAN
Company:
LILLY
Label History
Labels are not available on this site for HUMULIN BR, (NDA) 019529
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/10/1995
019
Manufacturing Change or Addition
3/26/1993
018
Labeling Revision
12/7/1992
017
Package Change
1/27/1992
016
Labeling Revision
3/12/1991
015
Labeling Revision
9/24/1990
014
Control Supplement
3/15/1989
013
Labeling Revision
1/23/1989
012
Labeling Revision
5/26/1989
011
Control Supplement
10/26/1988
010
Control Supplement
7/29/1988
009
Control Supplement
10/27/1987
007
Control Supplement
10/27/1987
005
Manufacturing Change or Addition
7/13/1987
004
Labeling Revision
7/28/1987
003
Labeling Revision
9/15/1986
002
Labeling Revision
5/28/1987
001
Control Supplement
4/28/1986
000
Approval
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test