Orange Book product · Generic (ANDA)
MINOXIDIL
MINOXIDIL
At a glance
Mar 03, 1987
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 03, 1987
39 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
MINOXIDIL
Strength
10MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 071345
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of MINOXIDIL
- 2006MEN'S ROGAINEBrand (NDA)
NDA 021812 · KENVUE BRANDS
- 1997ROGAINE EXTRA STRENGTH (FOR MEN)Brand (NDA)
NDA 020834 · KENVUE BRANDS
- 1996ROGAINE (FOR MEN)Brand (NDA)
NDA 019501 · KENVUE BRANDS
- —LONITENBrand (NDA)
NDA 018154 · PFIZER
- 2025MINOXIDIL EXTRA STRENGTH (FOR MEN)Generic (ANDA)
ANDA 217998 · TARO
- 2024MINOXIDIL (FOR WOMEN)Generic (ANDA)
ANDA 218175 · TARO
- 2024MINOXIDIL (FOR MEN)Generic (ANDA)
ANDA 218616 · AUROBINDO PHARMA
- 2018MINOXIDIL (FOR MEN)Generic (ANDA)
ANDA 209074 · TARO
- 2017MINOXIDIL (FOR MEN)Generic (ANDA)
ANDA 208092 · P AND L
- 2011MINOXIDILGeneric (ANDA)
ANDA 091344 · PERRIGO PHARMA INTL
- 2007THEROXIDILGeneric (ANDA)
ANDA 078176 · PURE SOURCE
- 2004THEROXIDILGeneric (ANDA)
ANDA 076239 · PURE SOURCE
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.
