Orange Book product · Brand (NDA)
QUINAGLUTE
QUINIDINE GLUCONATE
At a glance
Approved Prior to Jan 1, 1982
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
No patent or exclusivity dates are listed for this product.
Pharmaceutical detail
Active ingredient
QUINIDINE GLUCONATE
Strength
324MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
TE code
Not listed
Application
NDA 016647
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
Yes
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.
- 1989QUINIDINE GLUCONATEBrand (NDA)
NDA 007529 · LILLY
- —DURAQUINBrand (NDA)
NDA 017917 · WARNER CHILCOTT
- 2021QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 212589 · HIBROW HLTHCARE
- 1988QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 089894 · RISING
- 1987QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 089476 · HALSEY
- 1987QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 089338 · SUN PHARM INDUSTRIES
- 1986QUINALANGeneric (ANDA)
ANDA 088081 · CHARTWELL MOLECULAR
- 1985QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 089164 · SUPERPHARM
- 1985QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 088582 · ASCOT
- 1984QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 088431 · CYCLE
- 1983QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 087785 · WATSON LABS
- 1982QUINIDINE GLUCONATEGeneric (ANDA)
ANDA 087810 · ANI PHARMS
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.
