Orange Book product · Generic (ANDA)
CARBOPLATIN
CARBOPLATIN
At a glance
Oct 15, 2004
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Oct 15, 2004
22 yr ago
Today
Pharmaceutical detail
Active ingredient
CARBOPLATIN
Strength
50MG/5ML (10MG/ML)
Dosage form
INJECTABLE
Route
INTRAVENOUS
TE code
AP
Application
ANDA 077244
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.
