Orange Book product · Generic (ANDA)
METHYLPHENIDATE
METHYLPHENIDATE
Generic (ANDA)ANDA 210924TE ABRX ACTAVIS ELIZABETH
At a glance
Jun 19, 2020
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 19, 2020
6 yr 1 mo ago
Today
Pharmaceutical detail
Active ingredient
METHYLPHENIDATE
Strength
8.6MG
Dosage form
TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE
Route
ORAL
TE code
AB
Application
ANDA 210924
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of METHYLPHENIDATE
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.
