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:
IBUPROFEN
FDA Application No:
(ANDA) 074916
Active Ingredient(s):
IBUPROFEN
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for IBUPROFEN, (ANDA) 074916
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/25/2002
006
Control Supplement
8/3/2001
005
Labeling
4/25/2001
004
Manufacturing Revision
1/29/2001
003
Control Supplement
1/29/2001
002
Expiration Date Change
12/13/1999
001
Labeling
4/30/1999
000
Approval
Letter
1/9/1998
000
Tentative Approval
Letter
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test