Orange Book product · Generic (ANDA)
SODIUM ACETATE
SODIUM ACETATE
At a glance
Apr 17, 2026
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Apr 17, 2026
2 mo ago
Today
Pharmaceutical detail
Active ingredient
SODIUM ACETATE
Strength
100MEQ/50ML (2MEQ/ML)
Dosage form
SOLUTION
Route
INTRAVENOUS
TE code
AP
Application
ANDA 220274
Product number
001
Marketing status
RX
Reference listed drug (RLD)
No
Reference standard (RS)
No
Active-ingredient family
View full familyGeneric (ANDA) of SODIUM ACETATE
- 1983SODIUM ACETATEBrand (NDA)
NDA 018893 · HOSPIRA
- 2026SODIUM ACETATEGeneric (ANDA)
ANDA 218469 · AMNEAL
- 2025SODIUM ACETATEGeneric (ANDA)
ANDA 219826 · SOMERSET THERAPS LLC
- 2024SODIUM ACETATEGeneric (ANDA)
ANDA 216920 · HIKMA
- 2024SODIUM ACETATEGeneric (ANDA)
ANDA 214805 · MILLA PHARMS
- 2017SODIUM ACETATEGeneric (ANDA)
ANDA 206687 · FRESENIUS KABI 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.
