01 3Aspen Pharmacare Holdings
02 2Athena Pharmaceutiques
03 3Dr. 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 3Celogen Pharma Pvt. Ltd
17 4Chartwell Pharmaceuticals llc
18 4Clinect
19 4Concordia Labs Inc
20 1Cristalia Produtos Quimicos Farma. Ltda
21 3DURAMED PHARMS BARR
22 3Difgen
23 1Flagship Biotech International Pvt. Ltd
24 2Fresenius Kabi USA
25 2Generic Health
26 1Global Pharma Healthcare
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 4PH HEALTH
43 6Par Pharmaceutical
44 1Pharmachim AB
45 3Prinston
46 3Rising Pharmaceuticals Inc
47 1Rubicon Research
48 3SIVEM PHARMACEUTICALS ULC
49 3Sandoz B2B
50 1Somerset Pharmaceuticals Inc
51 3Sun Pharmaceutical Industries Limited
52 6Teva Pharmaceutical Industries
53 2Tris Pharma Inc
54 3Trupharma
55 6Unichem Laboratories Limited
56 3Unichem Pharmaceuticals USA, Inc
57 5Viatris
58 3Warner Chilcott Company, LLC
59 2XGen Pharmaceuticals
60 3Yung Shin Pharm Industrial
61 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 1Syrup
16 3TAB
17 14TABLET
18 22TABLET, EXTENDED RELEASE;ORAL
19 69TABLET;ORAL
20 10Tablet
21 8tablet
22 1Blank
01 60DISCN
02 11Generic
03 1Originator
04 60RX
05 43Blank
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 15Blank
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
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 : 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
