Orange Book product · Generic (ANDA)
ATOMOXETINE HYDROCHLORIDE
ATOMOXETINE HYDROCHLORIDE
At a glance
May 30, 2017
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 30, 2017
9 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
ATOMOXETINE HYDROCHLORIDE
Strength
EQ 10MG BASE
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 079022
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ATOMOXETINE HYDROCHLORIDE
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ANDA 078983 · APOTEX
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ANDA 079016 · AUROBINDO PHARMA
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ANDA 079019 · GLENMARK PHARMS LTD
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.
