Orange Book product · Generic (ANDA)
ATENOLOL
ATENOLOL
At a glance
Jan 28, 2005
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jan 28, 2005
21 yr 8 mo ago
Today
Pharmaceutical detail
Active ingredient
ATENOLOL
Strength
25MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 076900
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of ATENOLOL
- 1990TENORMINBrand (NDA)
NDA 018240 · TWI PHARMS
- 1989TENORMINBrand (NDA)
NDA 019058 · ASTRAZENECA
- 2019ATENOLOLGeneric (ANDA)
ANDA 213136 · UNICHEM
- 2009ATENOLOLGeneric (ANDA)
ANDA 078254 · NORTHSTAR HLTHCARE
- 2007ATENOLOLGeneric (ANDA)
ANDA 078512 · AUROBINDO PHARMA
- 2007ATENOLOLGeneric (ANDA)
ANDA 078210 · SUN PHARM INDS INC
- 2006ATENOLOLGeneric (ANDA)
ANDA 077877 · IPCA LABS LTD
- 2006ATENOLOLGeneric (ANDA)
ANDA 077443 · UNIQUE
- 2004ATENOLOLGeneric (ANDA)
ANDA 076907 · ABLE
- 2004ATENOLOLGeneric (ANDA)
ANDA 074056 · TEVA
- 1999ATENOLOLGeneric (ANDA)
ANDA 073457 · MYLAN
- 1998ATENOLOLGeneric (ANDA)
ANDA 074126 · MYLAN
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.
