Orange Book product · Generic (ANDA)
AMOXAPINE
AMOXAPINE
Generic (ANDA)ANDA 072691TE ABRX WATSON LABS
At a glance
Aug 28, 1992
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Aug 28, 1992
34 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
AMOXAPINE
Strength
25MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 072691
Product number
002
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of AMOXAPINE
- —ASENDINBrand (NDA)
NDA 018021 · LEDERLE
- 1991AMOXAPINEGeneric (ANDA)
ANDA 072879 · CHARTWELL RX
- 1989AMOXAPINEGeneric (ANDA)
ANDA 072418 · WATSON PHARMS TEVA
- 1989AMOXAPINEGeneric (ANDA)
ANDA 072419 · 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.
