Orange Book product · Generic (ANDA)
DROXIDOPA
DROXIDOPA
At a glance
Nov 01, 2021
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Nov 01, 2021
4 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
DROXIDOPA
Strength
100MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 215265
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of DROXIDOPA
- 2014NORTHERABrand (NDA)
NDA 203202 · LUNDBECK NA LTD
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- 2021DROXIDOPAGeneric (ANDA)
ANDA 214543 · SOMERSET THERAPS LLC
- 2021DROXIDOPAGeneric (ANDA)
ANDA 213033 · BIONPHARMA
- 2021DROXIDOPAGeneric (ANDA)
ANDA 213911 · ALKEM LABS LTD
- 2021DROXIDOPAGeneric (ANDA)
ANDA 214387 · AUROBINDO PHARMA LTD
- 2021DROXIDOPAGeneric (ANDA)
ANDA 212835 · HIKMA
- 2021DROXIDOPAGeneric (ANDA)
ANDA 214391 · JUBILANT CADISTA
- 2021DROXIDOPAGeneric (ANDA)
ANDA 211652 · LUPIN PHARMS
- 2021DROXIDOPAGeneric (ANDA)
ANDA 211741 · MSN PHARMS INC
- 2021DROXIDOPAGeneric (ANDA)
ANDA 214017 · SCIEGEN PHARMS
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.
