Orange Book product · Brand (NDA)
EPHEDRINE SULFATE
EPHEDRINE SULFATE
At a glance
Mar 01, 2017
Approved
Brand (NDA)
Application
Not listed
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Mar 01, 2017
9 yr 5 mo ago
Today
Pharmaceutical detail
Active ingredient
EPHEDRINE SULFATE
Strength
50MG/ML (50MG/ML)
Dosage form
SOLUTION
Route
INTRAVENOUS
TE code
Not listed
Application
NDA 208609
Product number
001
Marketing status
DISCN
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyThis is a brand (NDA) product. Other products sharing this active ingredient are listed below.
- 2023EMERPHEDBrand (NDA)
NDA 213407 · NEXUS
- 2022EPHEDRINE SULFATEBrand (NDA)
NDA 213994 · PH HEALTH
- 2021AKOVAZBrand (NDA)
NDA 208289 · EXELA PHARMA
- 2017CORPHEDRABrand (NDA)
NDA 208943 · PH HEALTH
- 2026EPHEDRINE SULFATEGeneric (ANDA)
ANDA 219991 · FRESENIUS KABI USA
- 2025EPHEDRINE SULFATEGeneric (ANDA)
ANDA 215593 · CIVICA
- 2025EPHEDRINE SULFATEGeneric (ANDA)
ANDA 218271 · FRESENIUS KABI USA
- 2025EPHEDRINE SULFATEGeneric (ANDA)
ANDA 218211 · GLAND
- 2024EPHEDRINE SULFATEGeneric (ANDA)
ANDA 217721 · HIKMA
- 2024EPHEDRINE SULFATEGeneric (ANDA)
ANDA 219050 · CAPLIN
- 2023EPHEDRINE SULFATEGeneric (ANDA)
ANDA 217276 · ZYDUS PHARMS
- 2023EPHEDRINE SULFATEGeneric (ANDA)
ANDA 214528 · SAGENT PHARMS INC
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.
