Orange Book product · Generic (ANDA)
QUININE SULFATE
QUININE SULFATE
Generic (ANDA)ANDA 203112TE ABRX LUPIN
At a glance
Apr 24, 2015
Approved
Generic (ANDA)
Application
AB
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 24, 2015
11 yr 4 mo ago
Today
Pharmaceutical detail
Active ingredient
QUININE SULFATE
Strength
324MG
Dosage form
CAPSULE
Route
ORAL
TE code
AB
Application
ANDA 203112
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
- 2012QUININE SULFATEGeneric (ANDA)
ANDA 202581 · AUROBINDO PHARMA USA
- 2012QUININE SULFATEGeneric (ANDA)
ANDA 091661 · TEVA 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.
