Orange Book product · Generic (ANDA)
QUINIDINE SULFATE
QUINIDINE SULFATE
At a glance
Jun 30, 1994
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Jun 30, 1994
32 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
QUINIDINE SULFATE
Strength
300MG
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
ANDA 040045
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of QUINIDINE SULFATE
- —QUINIDEXBrand (NDA)
NDA 012796 · WYETH PHARMS INC
- 1989QUINIDINE SULFATEGeneric (ANDA)
ANDA 081029 · SUN PHARM INDUSTRIES
- 1989QUINIDINE SULFATEGeneric (ANDA)
ANDA 081030 · SUN PHARM INDUSTRIES
- 1989QUINIDINE SULFATEGeneric (ANDA)
ANDA 081031 · SUN PHARM INDUSTRIES
- 1988QUINIDINE SULFATEGeneric (ANDA)
ANDA 089839 · CHARTWELL RX
- 1985QUINIDINE SULFATEGeneric (ANDA)
ANDA 088973 · SUPERPHARM
- 1982QUINIDINE SULFATEGeneric (ANDA)
ANDA 087909 · VANGARD
- 1982QUINIDINE SULFATEGeneric (ANDA)
ANDA 087837 · USL PHARMA
- —CIN-QUINGeneric (ANDA)
ANDA 085296 · SOLVAY
- —CIN-QUINGeneric (ANDA)
ANDA 085297 · SOLVAY
- —QUINIDINE SULFATEGeneric (ANDA)
ANDA 085103 · LILLY
- —CIN-QUINGeneric (ANDA)
ANDA 085299 · SOLVAY
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.
