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:
TOFRANIL
FDA Application No:
(NDA) 011838
Active Ingredient(s):
IMIPRAMINE HYDROCHLORIDE
Company:
NOVARTIS
Label History
Labels are not available on this site for TOFRANIL, (NDA) 011838
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/17/1998
034
Manufacturing Change or Addition
12/8/1992
032
Labeling Revision
12/24/1992
031
Control Supplement
11/27/1985
029
Control Supplement
5/13/1985
028
Control Supplement
4/29/1985
027
Labeling Revision
10/30/1984
026
Labeling Revision
5/1/1984
025
Labeling Revision
6/7/1983
023
Manufacturing Change or Addition
3/20/1981
022
Control Supplement
3/31/1980
021
Manufacturing Change or Addition
12/1/1978
020
Labeling Revision
10/2/1959
000
Approval
Other Important Information from FDA
There are no Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test