Orange Book product · Generic (ANDA)
CARBOPLATIN
CARBOPLATIN
At a glance
Apr 06, 2020
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 06, 2020
6 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
CARBOPLATIN
Strength
1GM/100ML (10MG/ML)
Dosage form
INJECTABLE
Route
INTRAVENOUS
TE code
Not listed
Application
ANDA 206775
Product number
005
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
Yes
Active-ingredient family
View full familyGeneric (ANDA) of CARBOPLATIN
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- 2026CARBOPLATINGeneric (ANDA)
ANDA 219999 · QILU PHARM HAINAN
- 2017CARBOPLATINGeneric (ANDA)
ANDA 208487 · INGENUS PHARMS LLC
- 2017CARBOPLATINGeneric (ANDA)
ANDA 207324 · GLAND
- 2016CARBOPLATINGeneric (ANDA)
ANDA 205487 · EUGIA PHARMA
- 2012CARBOPLATINGeneric (ANDA)
ANDA 091510 · NATCO PHARMA USA
- 2012CARBOPLATINGeneric (ANDA)
ANDA 078732 · ACTAVIS TOTOWA
- 2011CARBOPLATINGeneric (ANDA)
ANDA 091478 · PHARMOBEDIENT
- 2011CARBOPLATINGeneric (ANDA)
ANDA 091063 · PHARMOBEDIENT
- 2010CARBOPLATINGeneric (ANDA)
ANDA 091268 · EPIC PHARMA LLC
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.
