Orange Book product · Generic (ANDA)
CISPLATIN
CISPLATIN
At a glance
Aug 18, 2015
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 18, 2015
11 yr ago
Today
Pharmaceutical detail
Active ingredient
CISPLATIN
Strength
1MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 206774
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of CISPLATIN
- 1988CISPLATINBrand (NDA)
NDA 018057 · HQ SPCLT PHARMA
- 2024CISPLATINGeneric (ANDA)
ANDA 218868 · QILU
- 2017CISPLATINGeneric (ANDA)
ANDA 207323 · GLAND
- 2012CISPLATINGeneric (ANDA)
ANDA 091062 · PHARMOBEDIENT
- 2000CISPLATINGeneric (ANDA)
ANDA 074713 · BEDFORD
- 2000CISPLATINGeneric (ANDA)
ANDA 075036 · HIKMA
- 2000CISPLATINGeneric (ANDA)
ANDA 074656 · PHARMACHEMIE BV
- 2000CISPLATINGeneric (ANDA)
ANDA 074814 · TEVA PHARMS USA
- 1999CISPLATINGeneric (ANDA)
ANDA 074735 · FRESENIUS KABI USA
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.
