technique • Contamination can cause fever,
infection/sepsis, and/or other life-threatening
illness • Begin use promptly after opening;
Discard within specified time limit (See package
insert) • Do not use if contamination is suspected
SHAKE WELL BEFORE USING
US Pat
5,714,520
5,731,355
5,731,356
5,908,869
Dosage: See accompanying Professional
Information Brochure. Store between 4-22°C
(40-72°F). Do not freeze.
LOT
EXP
N363323-269-203
10
mg/mL propofol
Made in Italy
Unvarnished Area
Place an opaque white
box behind the laser box.
Laser box should be
Letter Press or Flexo Ink Only
Black
PMS 301 Blue
PMS 485 Red
Opaque White
Pattern Varnish
Material/Plate No.
00000-00
/APP402342A
CR # XXXXX
Plate Date
02/27/08 11:11 am SZT
Dimensions: 3-1/4" x 1-3/8"
Diprivan 1%
20 mL Vial Label
Notes to Printer:
Software: Illus. 11
Fonts: Helvetica Regular, Bold, Bold Oblique;
Helvetica Cond. Medium, Bold, Oblique;
OCRB; Symbol
Barcode:
The use of codes provided in artwork is optional;
replace if code specifications do not meet press requirements.
UPC - Magnification 85%, Bar Adjust -.002
Information encoded: 3 63323 269 20 3
AZ NDC 0310-0300-22
Dimensions: 9-19/32" x 7-21/32" x 1-7/8"
Material/Plate No.
00000-00
/APP62934A
CR # XXXXX
Plate Date
02/27/08 12:55 pm SZT
Software: Illus. 11.0
Fonts: Helvetica Regular, Bold, Oblique;
Bold Oblique; Helvetica Cond. Medium,
Bold, Oblique; Symbol; OCRB
Notes to Printer:
Barcode:
The use of codes provided in artwork
is optional; replace if code specifications do not
meet press requirements.
8-digit I 2 of 5 -
Magnification 54.7%,
Narrow Bar .0219, Ratio 2.5, Bar Adjust -.002
Information encoded: 00000000
14-digit I 2 of 5 -
Magnification 41.5%,
Narrow Bar .0200, Ratio 2.5, Bar Adjust -.002
Information encoded: 2 03 63323 269 50 4
HRC: E39
AZ NDC 0310-0300-50
Diprivan 1% 50 mL Vial Tray
Black
PMS 485 Red
PMS 301 Blue
Varnish
10
mg/mL propofol
®
®
propofol
INJECTABLE
EMULSION
NDC 63323-269-50
260950
10
mg/mL propofol
® ®
pro
pofo
l
INJECTABLE
EMULSION
NDC 63323-269-50
260950
10
mg/mL propofol
®®
pro
pofo
l
INJECTABLE
EMULSION
NDC 63323-269-50
260950
Twenty
50 mL single-patient
infusion vials
Sterile, nonpyrogenic
FOR I.V.
ADMINISTRATION
Twenty
50 mL single-patient
infusion vials
Ste
rile
, n
on
py
ro
ge
nic
FOR I.V. ADMINISTRATION
Twenty
50 mL single-patient
infusion vials
Ste
rile
, n
onp
yro
gen
ic
FOR I.V.
ADMINISTRATION
• Contains EDTA, which
inhibits micr obial growth
up to 12 hours
• Use strict aseptic technique
• Contamination can cause fever,
infection/sepsis, and/or other
life-threatening illness
• Begin use promptly after opening;
Discard within specified time limit
(See package insert)
• Do not use if contamination
is suspected
•
Contains EDT
A, which inhibits
micr
obial gr
owth up to 12 hours
•
Use strict aseptic technique
•
Contamination can cause fever
, infection/
sepsis, and/or other life-threatening illness
•
Begin use promptly after opening; Discard within specified time limit (See package insert)
•
Do not use if contamination is suspected
•
Contains EDT
A, which inhibits
micr
obial gr
owth up to 12 hours
•
Use strict aseptic technique
•
Contamination can cause fever
, infection/
sepsis, and/or other life-threatening illness
•
Begin use promptly after opening; Discard
within specified time limit (See package
insert)
•
Do not use if contamination is suspected
Man
uf
actured f
or
:
Made in Italy
DIPRIV
AN is a tr
ademar
k of
APP Phar
maceuticals
, LLC
.
62934A
Dosage:
See accompanying Professional Information Brochure.
In addition to the active component, propofol, the formulation contains: soybean oil (100 mg/mL), glycerol (22.5 mg/mL), egg lecithin (12 mg/mL) and disodium edetate (0.005%); with sodium hydroxide to adjust pH. DIPRIVAN
®
should be administered only by persons trained in the
administration of general anesthesia and not involved in the conduct of the surgical/diagnostic procedure. Facilities for maintenance of a patent airway, artificial ventilation, and oxygen enrichment and circulatory resuscitation must be immediately available. Store between 4-22°C (40-72°F).
Do not freeze.
SHAKE WELL BEFORE USING
Rx only
00000-00
00000-00
00000-00
2 03 63323 269 50 4
00000000
00000000
• Contains EDT
A, which
inhibits microbial gr
owth
up to 12 hours
• Use strict aseptic technique
• Contamination can cause fever
,
infection/sepsis, and/or other
life-threatening illness
• Begin use promptly after opening;
Discard within specified time limit
(See package insert)
• Do not use if contamination
is suspected
unvarnished area
US Pat 5,714,520 5,731,355
5,731,356 5,908,869
®
®
propofol
INJECTABLE
EMULSION
NDC 63323-269-50
260950
FOR I.V. ADMINISTRATION
50 mL single-patient infusion vial
10
mg/mL propofol
3
0
3
6
3
3
2
3
2
6
9
5
0
1
00000-00
402347A
LOT
EXP
Dosage: See accompanying Professional
Information Brochure. In addition to the
active component, propofol, the formu-
lation contains: soybean oil (100 mg/mL),
glycerol (22.5 mg/mL), egg lecithin
(12 mg/mL) and disodium edetate
(0.005%); with sodium hydroxide to
adjust pH. Store between 4-22°C
(40-72°F). Do not freeze.
Sterile, nonpyrogenic
• Contains EDTA, which
inhibits micr obial
gr owth up to 12 hours
• Use strict aseptic technique
• Contamination can cause
fever, infection/sepsis, and/or
other life-threatening illness
• Begin use promptly after
opening; Discard within
specified time limit (See
package insert)
• Do not use if contamination is
suspected
SHAKE WELL BEFORE USING
Rx only
Manufactured for:
Made in Italy
Black
PMS 301 Blue
PMS 485 Red
Opaque White
Pattern Varnish
Material/Plate No.
00000-00
/APP402347A
CR # XXXXX
Plate Date
02/27/08 11:15 am SZT
Dimensions: 1” x 5-7/16"
Diprivan 1%
50 mL Vial Label
Notes to Printer:
Software: Illus. 11
Fonts: Helvetica Regular, Bold, Bold Oblique;
Helvetica Cond. Medium, Bold, Oblique;
OCRB; Symbol
Barcode:
The use of codes provided in artwork is optional;
replace if code specifications do not meet press requirements.
14-digit I 2 of 5 - Magnification 18.0%, Narrow Bar .0072
Ratio 2.5, Bar Adjust -.002
Information encoded: 3 03 63323 269 50 1
AZ NDC 0310-0300-50
Material/Plate No.
00000-00/APP62936A
CR # XXXXXX
Plate Date
02/27/08 12:45 pm SZT
Software: Illus. 11.0
Fonts: Helvetica Regular, Bold, Bold Oblique;
Helvetica Cond. Medium, Bold, Oblique; Symbol;
OCRB
Notes to Printer:
Barcode:
The use of codes provided in artwork is optional;
replace if code specifications do not meet press requirements.
Bottom of Tray: 8-digit I 2 of 5 -
Magnification 54.7%,
Narrow Bar .0219, Ratio 2.5, Bar Adjust -.002
Information encoded: 00000000
Side of Tray: 14-digit I 2 of 5 -
Magnification 41.5%,
Narrow Bar .0166, Ratio 2.5, Bar Adjust -.002
Information encoded: 2 03 63323 269 65 8
HRC: D25
AZ NDC 0310-0300-11
Black (100% & 60%)
PMS 485 Red
PMS 301 Blue
Varnish
Diprivan 1% 100 mL Vial Tray
Dimensions: 9-19/32" x 3-27/32" x 3-1/4"
Rx only
Dosage:
See accompanying Professional Information Brochure.
In
addition to the active component, propofol, the formulation contains:
soybean oil (100 mg/mL), glycerol (22.5 mg/mL), egg lecithin (12 mg/mL) and disodium edetate (0.005%); with sodium hydroxide to adjust pH.
DIPRIVAN
®
should be administered only by persons trained in the admin-
istration of general anesthesia and not involved in the conduct of the surgical/ diagnostic procedure.
Facilities for maintenance of a patent airway, artificial
ventilation, and oxygen enrichment and circulatory resuscitation must be immediately available. Store between 4-22°C (40-72°F).
Do not freeze.
DIPRIVAN is a trademark of APP Pharmaceuticals, LLC.
00000-00
00000-00
00000-00
•
Contains EDT
A, which inhibits micr
obial gr
owth
up to 12 hours
•
Use strict aseptic technique
•
Contamination can cause fever
, infection/sepsis, and/or other
life-threatening illness
•
Begin use promptly after opening; Discard within specified time limit (See package insert)
•
Do not use if contamination is suspected
2 03 63323 269 65 8
SHAKE WELL BEFORE USING
Ten
100
mL
sin
gle
-pa
tie
nt i
nfu
sio
n v
ial
s
Ste
rile
, n
onp
yro
gen
ic
® ®
pro
pofo
l
INJECTABLE
EMULSION
FOR I.V. ADMINISTRATION
10
mg/mL propofol
Ten 100 mL
single-patient
infusion vials
Sterile, nonpyrogenic
•
Contains EDTA, which inhibits microbial
gr owth up to 12 hours
• Use strict aseptic technique
• Contamination can cause fever, infection/sepsis, and/or
other life-threatening illness
• Begin use promptly after opening; Discard within specified
time limit (See package insert)
• Do not use if contamination is suspected
®
®
propofol
INJECTABLE
EMULSION
FOR I.V. ADMINISTRATION
10
mg/mL propofol
NDC 63323-269-65
260965
NDC 63323-269-65
260965
NDC 63323-269-65
260965
®®
pro
pofo
l
INJECTABLE
EMULSION
FOR I.V. ADMINISTRATION
10
mg/mL propofol
62936A
Man
uf
actured f
or
:
Made in Italy
00000000
00000000
•
Contains EDT
A, which inhibits micr
obial gr
owth up to
12 hours
•
Use strict aseptic technique
•
Contamination can cause
fever
, infection/sepsis, and/or other life-threatening illness
•
Begin use
promptly after opening; Discard within specified time limit (Se
e package
insert)
•
Do not use if contamination is suspected
•
Contains EDTA, which inhibits micr
obial
growth up to 12 hours
• U
se
stri
ct a
sep
tic
tec
hni
que
• C
ont
am
ina
tio
n c
an
cau
se
fev
er,
inf
ect
ion
/se
psi
s, a
nd/
or
oth
er l
ife
-th
rea
ten
ing
illn
ess
• B
egi
n u
se
pro
mpt
ly
afte
r o
pen
ing
; D
isc
ard
with
in
spe
cifi
ed
tim
e l
im
it (
See
pac
kag
e i
nse
rt)
• D
o n
ot u
se
if c
ont
am
ina
tio
n i
s s
usp
ect
ed
Text in color block to be
printed in white. Number
one to be printed in white
with PMS 301 outline.
unvarnished area
FOR I.V. ADMINISTRATION
Rx only
100 mL single-patient infusion vial
Sterile, nonpyrogenic
00000-00
402348A
LOT
EXP
N
3
63323-269-65
4
Dosage: See accompanying Professional Information Brochure. In
addition to the active component, propofol, the formulation contains:
soybean oil (100 mg/mL), glycerol (22.5 mg/mL), egg lecithin (12 mg/mL)
and disodium edetate (0.005%); with sodium hydroxide to adjust pH.
Shake vial before use. Store between 4-22°C (40-72°F). Do not freeze.
•
Contains EDTA, which inhibits microbial growth
up to 12 hours
•
Use strict aseptic technique
•
Contamination can cause fever, infection/sepsis, and/or
other life-threatening illness
•
Begin use promptly after opening; Discard within
specified time limit (See package insert)
•
Do not use if contamination is suspected
SHAKE WELL BEFORE USING
US Pat 5,714,520
5,731,355
5,731,356
5,908,869
Manufactured for:
propofol
®
®
INJECTABLE
EMULSION
NDC 63323-269-65
260965
10
mg/mL propofol
Made in Italy
Dimensions: 2-1/4” x 5-7/16"
Material/Plate No.
00000-00
/APP402348A
CR # XXXXX
Plate Date
02/27/08 11:09 am SZT
Black
PMS 485 Red
PMS 301 Blue
Opaque White
Pattern Varnish
Diprivan 1% 100 mL Vial Label
Notes to Printer:
Software: Illus. 11.0
Fonts: Helvetica Regular, Bold, Bold Oblique;
Helvetica Cond. Medium, Bold, Oblique; Symbol;
OCRB
Barcode:
The use of codes provided in artwork is optional;
replace if code specifications do not meet press requirements.
12-digit UPC
- Magnification 100%, Bar Adjust -.002
Information encoded: 3 63323 269 65 4
AZ NDC 0310-0300-11
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