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 1Ananta Medicare
12 2Apotex Inc
13 3Ascent Innovative Medicines
14 3Aurobindo Pharma Limited
15 1Bluepharma
16 14Boehringer Ingelheim GmbH
17 4CONCORDIA PHARMS INC
18 3Celogen Pharma Pvt. Ltd
19 4Chartwell Pharmaceuticals llc
20 4Clinect
21 1Cristalia Produtos Quimicos Farma. Ltda
22 3DIFGEN PHARMS
23 3DURAMED PHARMS BARR
24 4ENDO OPERATIONS
25 1Flagship Biotech International Pvt. Ltd
26 2Fresenius Kabi USA
27 2Generic Health
28 2Hikma Pharmaceuticals
29 3Impax Laboratories
30 3Interpharm
31 1JAMP PHARMA
32 1Jubilant Generics
33 3LAVIPHARM LABS
34 1LP Pharmaceutical
35 1MARCAN PHARMACEUTICALS INC
36 3MINT PHARMACEUTICALS INC
37 1Magnus Pharma
38 1Medartuum AB
39 3Natco Pharma
40 1Novast Laboratories
41 1ORIFARM GROUP AS
42 1Omnia Pharmaceutical AB
43 6Par Pharmaceutical
44 1Pharmachim AB
45 3Prinston
46 3Rising Pharmaceuticals Inc
47 3SIVEM PHARMACEUTICALS ULC
48 3Sandoz B2B
49 1Somerset Pharmaceuticals Inc
50 3Sun Pharmaceutical Industries Limited
51 6Teva Pharmaceutical Industries
52 2Tris Pharma Inc
53 3Trupharma
54 6Unichem Laboratories Limited
55 3Unichem Pharmaceuticals USA, Inc
56 5Viatris
57 3Warner Chilcott Company, LLC
58 2XGen Pharmaceuticals
59 3Yung Shin Pharm Industrial
60 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 11Tablet
20 8tablet
21 1Blank
01 60DISCN
02 11Generic
03 1Originator
04 14Prescription
05 60RX
06 29Blank
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 1Clonidine
17 2Clonidine Lupin
18 2DURACLON
19 1Dixarit
20 1JAMP CLONIDINE
21 2JENLOGA
22 2KAPVAY
23 1LONID
24 1MAR-CLONIDINE
25 3MINT-CLONIDINE
26 2Menograine
27 1Menograine Drops
28 2NEXICLON XR
29 1ONYDA XR
30 3SANDOZ CLONIDINE
31 3TEVA-CLONIDINE
32 14Blank
01 8Australia
02 1Brazil
03 14Canada
04 14India
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 : 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 : 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 : 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
