Orange Book product · Generic (ANDA)
AMOXAPINE
AMOXAPINE
At a glance
Aug 01, 1989
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 01, 1989
37 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
AMOXAPINE
Strength
50MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 072419
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of AMOXAPINE
- —ASENDINBrand (NDA)
NDA 018021 · LEDERLE
- 1992AMOXAPINEGeneric (ANDA)
ANDA 072691 · WATSON LABS
- 1991AMOXAPINEGeneric (ANDA)
ANDA 072879 · CHARTWELL RX
- 1989AMOXAPINEGeneric (ANDA)
ANDA 072418 · WATSON PHARMS TEVA
- 1989AMOXAPINEGeneric (ANDA)
ANDA 072420 · WATSON PHARMS TEVA
- 1989AMOXAPINEGeneric (ANDA)
ANDA 072421 · WATSON PHARMS TEVA
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.
