Clonidine Transdermal System (Page 5 of 5)

PRINCIPAL DISPLAY PANEL — 0.1 mg/day

NDC 0591-3508 -04

Rx Only

Clonidine
Transdermal System, USP
0.1 mg/day*

*In vivo delivery of 0.1 mg clonidine per day for one week

To avoid possible burns, remove the clonidine transdermal system patch before
undergoing an MRI (magnetic resonance imaging) procedure.

For Transdermal Use Only -See package insert for dosage information.

4 Systems and 4 Adhesive Covers

1
(click image for full-size original)
2
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 0.2 mg/day

NDC 0591-3509 -04

Rx Only

Clonidine
Transdermal System, USP
0.2 mg/day*

*In vivo delivery of 0.2 mg clonidine per day for one week

To avoid possible burns, remove the clonidine transdermal system patch before
undergoing an MRI (magnetic resonance imaging) procedure.

For Transdermal Use Only -See package insert for dosage information.

4 Systems and 4 Adhesive Covers

3
(click image for full-size original)
4
(click image for full-size original)

PRINCIPAL DISPLAY PANEL — 0.3 mg/day

NDC 0591-3510- 04

Rx Only

Clonidine
Transdermal System, USP
0.3 mg/day*

*In vivo delivery of 0.3 mg clonidine per day for one week

To avoid possible burns, remove the clonidine transdermal system patch before
undergoing an MRI (magnetic resonance imaging) procedure.

For Transdermal Use Only -See package insert for dosage information.

4 Systems and 4 Adhesive Covers

5
(click image for full-size original)
6
(click image for full-size original)
CLONIDINE TRANSDERMAL SYSTEM clonidine patch
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0591-3508
Route of Administration TRANSDERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLONIDINE (CLONIDINE) CLONIDINE 0.1 mg in 1 d
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0591-3508-04 4 POUCH in 1 CARTON contains a POUCH (0591-3508-54)
1 NDC:0591-3508-54 1 PATCH in 1 POUCH This package is contained within the CARTON (0591-3508-04) and contains a PATCH
1 7 d in 1 PATCH This package is contained within a POUCH (0591-3508-54) and a CARTON (0591-3508-04)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090873 05/06/2014
CLONIDINE TRANSDERMAL SYSTEM clonidine patch
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0591-3509
Route of Administration TRANSDERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLONIDINE (CLONIDINE) CLONIDINE 0.2 mg in 1 d
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0591-3509-04 4 POUCH in 1 CARTON contains a POUCH (0591-3509-54)
1 NDC:0591-3509-54 1 PATCH in 1 POUCH This package is contained within the CARTON (0591-3509-04) and contains a PATCH
1 7 d in 1 PATCH This package is contained within a POUCH (0591-3509-54) and a CARTON (0591-3509-04)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090873 05/06/2014
CLONIDINE TRANSDERMAL SYSTEM clonidine patch
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0591-3510
Route of Administration TRANSDERMAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLONIDINE (CLONIDINE) CLONIDINE 0.3 mg in 1 d
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0591-3510-04 4 POUCH in 1 CARTON contains a POUCH (0591-3510-54)
1 NDC:0591-3510-54 1 PATCH in 1 POUCH This package is contained within the CARTON (0591-3510-04) and contains a PATCH
1 7 d in 1 PATCH This package is contained within a POUCH (0591-3510-54) and a CARTON (0591-3510-04)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090873 05/06/2014
Labeler — Actavis Pharma, Inc. (119723554)

Revised: 12/2020 Actavis Pharma, Inc.

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