Orange Book product · Generic (ANDA)
PENTAMIDINE ISETHIONATE
PENTAMIDINE ISETHIONATE
At a glance
Dec 18, 1995
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Dec 18, 1995
30 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
PENTAMIDINE ISETHIONATE
Strength
300MG/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 073617
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of PENTAMIDINE ISETHIONATE
- 1989NEBUPENTBrand (NDA)
NDA 019887 · FRESENIUS KABI USA
- 1984PENTAMBrand (NDA)
NDA 019264 · FRESENIUS KABI USA
- 2023PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 206983 · X-GEN PHARMS INC
- 2022PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 206982 · PHARMOBEDIENT
- 2021PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 213806 · AVET LIFESCIENCES
- 2019PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 206667 · PAI HOLDINGS
- 2017PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 206666 · PAI HOLDINGS
- 1995PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 074303 · WATSON LABS
- 1994PENTACARINATGeneric (ANDA)
ANDA 073447 · ARMOUR PHARM
- 1992PENTAMIDINE ISETHIONATEGeneric (ANDA)
ANDA 073479 · HOSPIRA
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.
