Orange Book product · Generic (ANDA)
ROPINIROLE HYDROCHLORIDE
ROPINIROLE HYDROCHLORIDE
At a glance
Jun 01, 2009
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 01, 2009
17 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
ROPINIROLE HYDROCHLORIDE
Strength
EQ 0.25MG BASE
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 090411
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ROPINIROLE HYDROCHLORIDE
- 2008REQUIP XLBrand (NDA)
NDA 022008 · GLAXOSMITHKLINE LLC
- 1997REQUIPBrand (NDA)
NDA 020658 · GLAXOSMITHKLINE LLC
- 2025ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 217862 · ELITE LABS INC
- 2022ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 204413 · PRINSTON INC
- 2017ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 204022 · ACCORD HLTHCARE
- 2013ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 202786 · ALEMBIC
- 2012ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 079229 · ORBION PHARMS
- 2012ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 200462 · AUROBINDO PHARMA USA
- 2012ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 091395 · CHARTWELL RX
- 2012ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 201576 · DR REDDYS LABS LTD
- 2012ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 201047 · SANDOZ INC
- 2012ROPINIROLE HYDROCHLORIDEGeneric (ANDA)
ANDA 200431 · WATSON LABS INC
Listed patents
No patents are listed against this product in the Orange Book. Listed patents reflect those the NDA holder submits under 21 U.S.C. 355 and are not exhaustive.

