Orange Book product · Generic (ANDA)
POLYMYXIN B SULFATE
POLYMYXIN B SULFATE
At a glance
Sep 30, 1994
Approved
Generic (ANDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 30, 1994
32 yr 2 mo ago
Today
Pharmaceutical detail
Active ingredient
POLYMYXIN B SULFATE
Strength
EQ 500,000 UNITS BASE/VIAL
Dosage form
INJECTABLE
Route
INJECTION
TE code
Not listed
Application
ANDA 063000
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of POLYMYXIN B SULFATE
- 2016POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 207322 · GLAND
- 2016POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 206589 · EUGIA PHARMA
- 2014POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 202766 · XELLIA PHARMS APS
- 2011POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 090110 · RISING
- 2008POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 065372 · FRESENIUS KABI USA
- 1983POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 062455 · PADDOCK LLC
- —AEROSPORINGeneric (ANDA)
ANDA 062036 · GLAXOSMITHKLINE
- —POLYMYXIN B SULFATEGeneric (ANDA)
ANDA 060716 · HIKMA
- —POLY-RXGeneric (ANDA)
ANDA 061578 · X GEN 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.
