Orange Book product · Brand (NDA)
OXALIPLATIN
OXALIPLATIN
At a glance
Aug 07, 2009
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 07, 2009
17 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
OXALIPLATIN
Strength
100MG/20ML (5MG/ML)
Dosage form
INJECTABLE
Route
INTRAVENOUS
TE code
Not listed
Application
NDA 022160
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 2005ELOXATINBrand (NDA)
NDA 021759 · SANOFI AVENTIS US
- 2002ELOXATINBrand (NDA)
NDA 021492 · SANOFI AVENTIS US
- 2026OXALIPLATINGeneric (ANDA)
ANDA 219765 · SHANDONG
- 2025OXALIPLATINGeneric (ANDA)
ANDA 217925 · HETERO LABS LTD VI
- 2024OXALIPLATINGeneric (ANDA)
ANDA 217348 · MEITHEAL
- 2018OXALIPLATINGeneric (ANDA)
ANDA 207562 · INGENUS PHARMS LLC
- 2018OXALIPLATINGeneric (ANDA)
ANDA 204880 · ACTAVIS
- 2017OXALIPLATINGeneric (ANDA)
ANDA 205529 · EUGIA PHARMA
- 2017OXALIPLATINGeneric (ANDA)
ANDA 207385 · GLAND
- 2017OXALIPLATINGeneric (ANDA)
ANDA 204378 · AM REGENT
- 2017OXALIPLATINGeneric (ANDA)
ANDA 207474 · ACCORD HLTHCARE
- 2017OXALIPLATINGeneric (ANDA)
ANDA 208523 · CHARTWELL MOLECULAR
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.
