Orange Book product · Generic (ANDA)
SULINDAC
SULINDAC
At a glance
Apr 03, 1990
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 03, 1990
36 yr 9 mo ago
Today
Pharmaceutical detail
Active ingredient
SULINDAC
Strength
150MG
Dosage form
TABLET
Route
ORAL
TE code
AB
Application
ANDA 071891
Product number
001
Marketing status
RX
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
- 1992SULINDACGeneric (ANDA)
ANDA 072973 · ANI PHARMS
- 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 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.
