Orange Book product · Generic (ANDA)
CARBOPLATIN
CARBOPLATIN
At a glance
Jan 18, 2007
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 18, 2007
19 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
CARBOPLATIN
Strength
50MG/5ML (10MG/ML)
Dosage form
INJECTABLE
Route
INTRAVENOUS
TE code
AP
Application
ANDA 077861
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
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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.
