Orange Book product · Generic (ANDA)
QUININE SULFATE
QUININE SULFATE
Generic (ANDA)ANDA 091661TE ABRX TEVA PHARMS
At a glance
Sep 28, 2012
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 28, 2012
13 yr 11 mo ago
Today
Pharmaceutical detail
Active ingredient
QUININE SULFATE
Strength
324MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 091661
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of QUININE SULFATE
- 2005QUALAQUINBrand (NDA)
NDA 021799 · SUN PHARM INDUSTRIES
- 2015QUININE SULFATEGeneric (ANDA)
ANDA 204372 · INGENUS PHARMS LLC
- 2015QUININE SULFATEGeneric (ANDA)
ANDA 203729 · AMNEAL PHARMS
- 2015QUININE SULFATEGeneric (ANDA)
ANDA 203112 · LUPIN
- 2012QUININE SULFATEGeneric (ANDA)
ANDA 202581 · AUROBINDO PHARMA USA
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.
