Orange Book product · Generic (ANDA)
SULINDAC
SULINDAC
At a glance
Feb 28, 1992
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Feb 28, 1992
34 yr 10 mo ago
Today
Pharmaceutical detail
Active ingredient
SULINDAC
Strength
150MG
Dosage form
TABLET
Route
ORAL
TE code
Not listed
Application
ANDA 072973
Product number
002
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SULINDAC
- —CLINORILBrand (NDA)
NDA 017911 · MERCK
- 1993SULINDACGeneric (ANDA)
ANDA 073039 · RISING
- 1991SULINDACGeneric (ANDA)
ANDA 073262 · EPIC PHARMA LLC
- 1991SULINDACGeneric (ANDA)
ANDA 072712 · CHARTWELL RX
- 1991SULINDACGeneric (ANDA)
ANDA 072713 · CHARTWELL RX
- 1991SULINDACGeneric (ANDA)
ANDA 072050 · SUN PHARM INDUSTRIES
- 1991SULINDACGeneric (ANDA)
ANDA 072051 · SUN PHARM INDUSTRIES
- 1991SULINDACGeneric (ANDA)
ANDA 072711 · EPIC PHARMA
- 1990SULINDACGeneric (ANDA)
ANDA 071891 · WATSON LABS
- 1990SULINDACGeneric (ANDA)
ANDA 071795 · WATSON LABS
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.
