Orange Book product · Generic (ANDA)
FUROSEMIDE
FUROSEMIDE
At a glance
May 28, 1999
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
May 28, 1999
27 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
FUROSEMIDE
Strength
10MG/ML
Dosage form
INJECTABLE
Route
INJECTION
TE code
AP
Application
ANDA 075241
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of FUROSEMIDE
- 2025LASIX ONYUBrand (NDA)
NDA 217294 · SQ INNOVATION
- 2022FUROSCIXBrand (NDA)
NDA 209988 · SCPHARMACEUTICALS
- 1984FUROSEMIDEBrand (NDA)
NDA 019036 · ABRAXIS PHARM
- 1984FUROSEMIDEBrand (NDA)
NDA 018750 · EPIC PHARMA LLC
- 1984FUROSEMIDEBrand (NDA)
NDA 018902 · FRESENIUS KABI USA
- 1983FUROSEMIDEBrand (NDA)
NDA 018579 · AM REGENT
- 1983FUROSEMIDEBrand (NDA)
NDA 018413 · CHARTWELL RX
- 1982FUROSEMIDEBrand (NDA)
NDA 018507 · ABRAXIS PHARM
- 1982FUROSEMIDEBrand (NDA)
NDA 018415 · ESJAY PHARMA
- 1982FUROSEMIDEBrand (NDA)
NDA 018670 · WYETH AYERST
- 1982FUROSEMIDEBrand (NDA)
NDA 018667 · HOSPIRA
- 1982FUROSEMIDEBrand (NDA)
NDA 018420 · WARNER CHILCOTT
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.
