01 12Accord healthcare
02 10Actavis Inc
03 12Alembic Pharmaceuticals Limited
04 11Aurobindo Pharma Limited
05 12Chartwell Pharmaceuticals llc
06 5Cinfa
07 7Cosette Pharma
08 3DOC Generici
09 8EG SpA
10 7Epic Pharma. LLC.
11 24GSK
12 7Glenmark Pharmaceuticals
13 7Hikma Pharmaceuticals
14 8Kern Pharma S.L.
15 9Krka
16 8LABORATOIRE GLAXOSMITHKLINE
17 4LABORATORIOS NORMON SA
18 7MLV
19 7OrBion Pharmaceuticals
20 7Orchid Pharma
21 7PHARMOBEDIENT
22 4Pharmascience Inc.
23 12Prinston
24 3STADA Arzneimittel
25 11Sandoz B2B
26 4Sun Pharmaceutical Industries Limited
27 5Tarbis Farma Sl
28 13Teva Pharmaceutical Industries
29 5Viatris
30 5XYZ Pharma
31 7Zydus Lifesciences
01 27Extended-Release Tablet
02 27Film Coated Tablet
03 3Ropinirol 0.25Mg 21 Combined Oral Use
04 3Ropinirol 0.5Mg 21 Combined Oral Use
05 3Ropinirol 1Mg 21 Combined Oral Use
06 3Ropinirol 2Mg 21 Combined Oral Use
07 6Ropinirol 2Mg 28 Combined Oral Use Rp
08 7Ropinirol 4Mg 28 Combined Oral Use Rp
09 3Ropinirol 5Mg 21 Combined Oral Use
10 7Ropinirol 8Mg 28 Combined Oral Use Rp
11 5TAB
12 19TABLET
13 47TABLET, EXTENDED RELEASE;ORAL
14 91TABLET;ORAL
01 31Authorized
02 23Cancelled
03 52DISCN
04 5Generic
05 7Generic EU CTD
06 12Prescription
07 86RX
08 35Blank
01 1Accord Ropinirole 0.25 mg
02 1Accord Ropinirole 0.5 mg
03 1Accord Ropinirole 1 mg
04 1Accord Ropinirole 2 mg
05 1Accord Ropinirole 5 mg
06 3Adartrel
07 4PMS-ROPINIROLE
08 7REQUIP
09 6REQUIP XL
10 125ROPINIROLE HYDROCHLORIDE
11 8Reqp
12 5Requip
13 3Requip-Prolib
14 3Rolpryna Sr
15 27Ropinirol
16 3Ropinirol Aurobindo
17 5Ropinirol Cinfa
18 8Ropinirol Kern Pharma
19 3Ropinirol Krka
20 4Ropinirol Normon
21 3Ropinirol Prolib Sandoz
22 3Ropinirol Ratiopharm
23 3Ropinirol Stada
24 5Ropinirol Tarbis
25 3Ropinirole Teva
26 4SPC-ROPINIROLE
27 4TEVA-ROPINIROLE
28 7Blank
01 12Canada
02 7India
03 35Italy
04 5South Africa
05 54Spain
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
