01 3Aspen Pharmacare Holdings
02 2Athena Pharmaceutiques
03 4Dr. Reddy's Laboratories
04 12care4 ApS
05 3A&M Therapy
06 16Actavis Inc
07 1Ajanta Pharma Limited
08 3Alembic Pharmaceuticals Limited
09 2American Regent
10 1Amneal Pharmaceuticals
11 2Apotex Inc
12 3Ascent Innovative Medicines
13 3Aurobindo Pharma Limited
14 1Bluepharma
15 14Boehringer Ingelheim GmbH
16 4CONCORDIA PHARMS INC
17 3Celogen Pharma Pvt. Ltd
18 4Chartwell Pharmaceuticals llc
19 4Clinect
20 1Cristalia Produtos Quimicos Farma. Ltda
21 3DIFGEN PHARMS
22 3DURAMED PHARMS BARR
23 4ENDO OPERATIONS
24 1Flagship Biotech International Pvt. Ltd
25 2Fresenius Kabi USA
26 2Generic Health
27 2Hikma Pharmaceuticals
28 3Impax Laboratories
29 3Interpharm
30 1JAMP PHARMA
31 1Jubilant Generics
32 3LAVIPHARM LABS
33 1LP Pharmaceutical
34 1MARCAN PHARMACEUTICALS INC
35 3MINT PHARMACEUTICALS INC
36 1Magnus Pharma
37 1Medartuum AB
38 3Natco Pharma
39 1Novast Laboratories
40 1ORIFARM GROUP AS
41 1Omnia Pharmaceutical AB
42 6Par Pharmaceutical
43 1Pharmachim AB
44 3Prinston
45 3Rising Pharmaceuticals Inc
46 3SIVEM PHARMACEUTICALS ULC
47 3Sandoz B2B
48 1Somerset Pharmaceuticals Inc
49 3Sun Pharmaceutical Industries Limited
50 6Teva Pharmaceutical Industries
51 2Tris Pharma Inc
52 3Trupharma
53 6Unichem Laboratories Limited
54 3Unichem Pharmaceuticals USA, Inc
55 5Viatris
56 3Warner Chilcott Company, LLC
57 2XGen Pharmaceuticals
58 3Yung Shin Pharmaceutical Industrial
59 2Zydus Pharmaceuticals
01 1Antic-calc Tablet, drasjert
02 1Clonidine 0.15Mg 1Ml 5 Units Parenteral Use
03 1Clonidine 2,5Mg 2 Plasters Transdermal Use
04 1Clonidine 300Mcg 30 Joined' Oral Use
05 1Clonidine 5Mg 2 Plasters Transdermal Use
06 1DRP
07 1E R Tablet
08 3ER Film
09 12INJECTABLE;INJECTION
10 1INJECTION
11 1Injection
12 6SOLUTION FOR INJECTION
13 2SUSPENSION, EXTENDED RELEASE;ORAL
14 15SYSTEM;TRANSDERMAL
15 3TAB
16 14TABLET
17 22TABLET, EXTENDED RELEASE;ORAL
18 69TABLET;ORAL
19 10Tablet
20 8tablet
21 1Blank
01 61DISCN
02 11Generic
03 1Originator
04 14Prescription
05 59RX
06 28Blank
01 2APO-Clonidine
02 3CATAPRES
03 1CATAPRES-TTS-1
04 1CATAPRES-TTS-2
05 1CATAPRES-TTS-3
06 1CLONIDIN
07 16CLONIDINE
08 83CLONIDINE HYDROCHLORIDE
09 3CLONIDINE HYDROCHLORIDE AND CHLORTHALIDONE
10 3CLORPRES
11 3COMBIPRES
12 7Catapres
13 2Catapres 100
14 5Catapresan
15 2Catapresan Tts
16 2Clonidine Lupin
17 2DURACLON
18 1Dixarit
19 1JAMP CLONIDINE
20 2JENLOGA
21 2KAPVAY
22 1LONID
23 1MAR-CLONIDINE
24 3MINT-CLONIDINE
25 2Menograine
26 1Menograine Drops
27 2NEXICLON XR
28 1ONYDA XR
29 3SANDOZ CLONIDINE
30 3TEVA-CLONIDINE
31 14Blank
01 8Australia
02 1Brazil
03 14Canada
04 13India
05 5Italy
06 1Nepal
07 1Norway
08 1Portugal
09 4South Africa
10 6Sweden
11 120USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Menograine Drops
Dosage Form : DRP
Dosage Strength : 25mg / 0.5ml
Packaging : 5X1mg / 0.5ml
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
Regulatory Info : RX
Registration Country : USA
Brand Name : NEXICLON XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 0.17MG BASE
Packaging :
Approval Date : 2009-12-03
Application Number : 22500
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : CLONIDINE
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.1MG/24HR
Packaging :
Approval Date : 2010-08-20
Application Number : 79090
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Menograine
Dosage Form : TAB
Dosage Strength : 25mcg
Packaging : 100X1mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Menograine
Dosage Form : TAB
Dosage Strength : 25mcg
Packaging : 30X1mcg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Athena Pharmaceutiques is a Partner of Choice for Drug Delivery & Life Cycle Management.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : NEXICLON XR
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 0.26MG BASE
Packaging :
Approval Date : 2009-12-03
Application Number : 22500
Regulatory Info : DISCN
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : CLONIDINE
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.2MG/24HR
Packaging :
Approval Date : 2010-08-20
Application Number : 79090
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
Brand Name : CLONIDINE
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.3MG/24HR
Packaging :
Approval Date : 2010-08-20
Application Number : 79090
Regulatory Info : RX
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2018-04-30
Application Number : 210680
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 1987-03-23
Application Number : 70395
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 1987-03-23
Application Number : 70396
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CATAPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17407
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CATAPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17407
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CATAPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17407
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Brand Name : COMBIPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG;0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17503
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Brand Name : COMBIPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG;0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-01-01
Application Number : 17503
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
CHLORTHALIDONE; CLONIDINE HYDROCHLORIDE
Brand Name : COMBIPRES
Dosage Form : TABLET;ORAL
Dosage Strength : 15MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1984-04-10
Application Number : 17503
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : JENLOGA
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 0.1MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-09-30
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : JENLOGA
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2010-05-25
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KAPVAY
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 2010-09-28
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : KAPVAY
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 0.2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2010-09-28
Application Number : 22331
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CATAPRES-TTS-1
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.1MG/24HR
Packaging :
Approval Date : 1984-10-10
Application Number : 18891
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CATAPRES-TTS-2
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.2MG/24HR
Packaging :
Approval Date : 1984-10-10
Application Number : 18891
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : CATAPRES-TTS-3
Dosage Form : SYSTEM;TRANSDERMAL
Dosage Strength : 0.3MG/24HR
Packaging :
Approval Date : 1984-10-10
Application Number : 18891
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.3MG
Packaging :
Approval Date : 1987-06-09
Application Number : 70317
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.1MG
Packaging :
Approval Date : 1987-07-09
Application Number : 70317
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 0.2MG
Packaging :
Approval Date : 1987-06-09
Application Number : 70317
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : CLONIDINE
Dosage Form : SUSPENSION, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 0.09MG BASE/ML
Packaging :
Approval Date : 2009-12-03
Application Number : 22499
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : DURACLON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 1MG/10ML (0.1MG/ML)
Packaging :
Approval Date : 1996-10-02
Application Number : 20615
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : DURACLON
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : 5MG/10ML (0.5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-04-27
Application Number : 20615
Regulatory Info : DISCN
Registration Country : USA
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