01 12Accord healthcare
02 10Actavis Inc
03 12Alembic Pharmaceuticals Limited
04 2Aurobindo Pharma Limited
05 12Chartwell Pharmaceuticals llc
06 7Cosette Pharma
07 3DOC Generici
08 8EG SpA
09 7Epic Pharma. LLC.
10 28GSK
11 7Glenmark Pharmaceuticals
12 7Hikma Pharmaceuticals
13 3KRKA Sverige AB
14 3Krka
15 8LABORATOIRE GLAXOSMITHKLINE
16 7MLV
17 7NORVIUM BIOSCIENCE
18 7OrBion Pharmaceuticals
19 7Orchid Pharma
20 4Pharmascience Inc.
21 12Prinston
22 4RANBAXY LABORATORIES LIMITED
23 1STADA Arzneimittel
24 11Sandoz B2B
25 10Teva Pharmaceutical Industries
26 11Viatris
27 5XYZ Pharma
28 7Zydus Lifesciences
01 12DEPOTTABLETT
02 3FILM COATED PILL
03 10FILMDRAGERAD TABLETT
04 3Ropinirol 0.25Mg 21 Combined Oral Use
05 3Ropinirol 0.5Mg 21 Combined Oral Use
06 3Ropinirol 1Mg 21 Combined Oral Use
07 3Ropinirol 2Mg 21 Combined Oral Use
08 6Ropinirol 2Mg 28 Combined Oral Use Rp
09 7Ropinirol 4Mg 28 Combined Oral Use Rp
10 3Ropinirol 5Mg 21 Combined Oral Use
11 7Ropinirol 8Mg 28 Combined Oral Use Rp
12 5TAB
13 19TABLET
14 47TABLET, EXTENDED RELEASE;ORAL
15 91TABLET;ORAL
01 52DISCN
02 5Generic
03 7Generic EU CTD
04 12Prescription
05 86RX
06 60Blank
01 3ADARTREL
02 1Accord Ropinirole 0.25 mg
03 1Accord Ropinirole 0.5 mg
04 1Accord Ropinirole 1 mg
05 1Accord Ropinirole 2 mg
06 1Accord Ropinirole 5 mg
07 4PMS-ROPINIROLE
08 4RAN-ROPINIROLE
09 7REQUIP
10 6REQUIP XL
11 125ROPINIROLE HYDROCHLORIDE
12 8Reqp
13 5Requip
14 3Requip Depot
15 27Ropinirol
16 3Ropinirol Krka
17 3Ropinirol Sandoz
18 1Ropinirol Stada
19 3Ropinirole Teva
20 4TEVA-ROPINIROLE
21 4Vunexin
22 7Blank
01 12Canada
02 7India
03 35Italy
04 5South Africa
05 25Sweden
06 138USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.25MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 3MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2008-05-19
Application Number : 77460
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-09-19
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-09-19
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-09-19
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-09-19
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1997-09-19
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-01-27
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-01-27
Application Number : 20658
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2008-06-13
Application Number : 22008
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2008-06-13
Application Number : 22008
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2008-06-13
Application Number : 22008
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2008-06-13
Application Number : 22008
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 12MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2008-10-31
Application Number : 22008
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : REQUIP XL
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2009-04-10
Application Number : 22008
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.25MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 3MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 5MG BASE
Packaging :
Approval Date : 2008-05-19
Application Number : 77852
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.25MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 78110
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 0.5MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 78110
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ROPINIROLE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2008-05-05
Application Number : 78110
Regulatory Info : RX
Registration Country : USA
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