Orange Book product · Generic (ANDA)
PROPOFOL
PROPOFOL
At a glance
Oct 12, 2021
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 12, 2021
4 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
PROPOFOL
Strength
10MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AB
Application
ANDA 206408
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PROPOFOL
- 1989DIPRIVANBrand (NDA)
NDA 019627 · FRESENIUS KABI USA
- 2025PROPOFOLGeneric (ANDA)
ANDA 217945 · EMERGE BIOSCIENCE
- 2024PROPOFOLGeneric (ANDA)
ANDA 217525 · AMNEAL
- 2024PROPOFOLGeneric (ANDA)
ANDA 217013 · ASPIRO
- 2020PROPOFOLGeneric (ANDA)
ANDA 205576 · INNOPHARMA
- 2018PROPOFOLGeneric (ANDA)
ANDA 205067 · DR REDDYS
- 2015PROPOFOLGeneric (ANDA)
ANDA 205307 · WATSON LABS INC
- 2006PROPOFOLGeneric (ANDA)
ANDA 077908 · HOSPIRA
- 2005PROPOFOLGeneric (ANDA)
ANDA 074848 · HIKMA
- 2000PROPOFOLGeneric (ANDA)
ANDA 075392 · TEVA PARENTERAL
- 1999PROPOFOLGeneric (ANDA)
ANDA 075102 · SAGENT PHARMS 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.
