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:
REPREXAIN
FDA Application No:
(ANDA) 076642
Active Ingredient(s):
HYDROCODONE BITARTRATE; IBUPROFEN
Company:
INTERPHARM
Label History
Labels are not available on this site for REPREXAIN, (ANDA) 076642
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/19/2007
008
Labeling
Letter
10/19/2007
007
Chemistry New Strength
Letter
10/19/2007
006
Labeling
Letter
10/19/2007
005
Chemistry New Strength
Letter
10/12/2004
003
Supplement
3/18/2004
000
Tentative Approval
3/18/2004
000
Approval
There are no Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test