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01 3Aspen Pharmacare Holdings
02 2Athena Pharmaceutiques
03 3Dr. Reddy's Laboratories
04 22care4
05 3A&M Therapy
06 1Abboxia Ab
07 16Actavis Inc
08 1Ajanta Pharma Limited
09 3Alembic Pharmaceuticals Limited
10 2American Regent
11 1Amneal Pharmaceuticals
12 2Apotex Inc
13 3Ascent Innovative Medicines
14 3Aurobindo Pharma Limited
15 1Bluepharma
16 15Boehringer Ingelheim GmbH
17 3Celogen Pharma Pvt. Ltd
18 4Chartwell Pharmaceuticals llc
19 4Clinect
20 4Concordia Labs Inc
21 2Cps Cito Pharma Services Gmbh
22 1Cristalia Produtos Quimicos Farma. Ltda
23 3DURAMED PHARMS BARR
24 3Difgen
25 5Ebb Medical
26 1Flagship Biotech International Pvt. Ltd
27 2Fresenius Kabi USA
28 2Generic Health
29 1Glenwood Gmbh Pharmazeutiche Erzeugnisse
30 1Global Pharma Healthcare
31 2Hikma Pharmaceuticals
32 3Impax Laboratories
33 3Interpharm
34 1JAMP PHARMA
35 1Jubilant Generics
36 3LAVIPHARM LABS
37 1LP Pharmaceutical
38 1MARCAN PHARMACEUTICALS INC
39 3MINT PHARMACEUTICALS INC
40 1Macure Pharma
41 1Magnus Pharma
42 1Medartuum
43 3Natco Pharma
44 1Novast Laboratories
45 7ORIFARM GROUP AS
46 4PH HEALTH
47 6Par Pharmaceutical
48 2Paranova Pharmaceuticals Ab
49 3Prinston
50 3Rising Pharmaceuticals Inc
51 1Rubicon Research
52 3SIVEM PHARMACEUTICALS ULC
53 3Sandoz B2B
54 1Somerset Pharmaceuticals Inc
55 3Sun Pharmaceutical Industries Limited
56 6Teva Pharmaceutical Industries
57 2Tris Pharma Inc
58 3Tulex Pharmaceutical
59 6Unichem Laboratories Limited
60 3Unichem Pharmaceuticals USA, Inc
61 5Viatris
62 3Warner Chilcott Company, LLC
63 2XGen Pharmaceuticals
64 3Yung Shin Pharm Industrial
65 2Zydus Pharmaceuticals
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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 21Injectable Solution
12 1Injection
13 2SUSPENSION, EXTENDED RELEASE;ORAL
14 15SYSTEM;TRANSDERMAL
15 1Syrup
16 3TAB
17 14TABLET
18 22TABLET, EXTENDED RELEASE;ORAL
19 69TABLET;ORAL
20 13Tablet
21 8tablet
22 1Blank
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01 2Allowed
02 10Approved
03 60DISCN
04 12Deregistered
05 11Generic
06 1Originator
07 14Prescription
08 60RX
09 23Blank
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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 1Caruxin
13 8Catapres
14 2Catapres 100
15 18Catapresan
16 2Catapresan Tts
17 2Clonidine Lupin
18 1Clotaxip
19 2DURACLON
20 1Dixarit
21 1JAMP CLONIDINE
22 2JENLOGA
23 2KAPVAY
24 2Klonidin Paranova
25 1LONID
26 1MAR-CLONIDINE
27 3MINT-CLONIDINE
28 2Menograine
29 1Menograine Drops
30 2NEXICLON XR
31 1ONYDA XR
32 3SANDOZ CLONIDINE
33 3TEVA-CLONIDINE
34 15Blank
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01 8Australia
02 1Brazil
03 14Canada
04 14India
05 5Italy
06 1Nepal
07 1Norway
08 1Portugal
09 4South Africa
10 22Sweden
11 2Switzerland
12 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
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
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