Orange Book product · Generic (ANDA)
SODIUM ACETATE
SODIUM ACETATE
Generic (ANDA)ANDA 219826TE APRX SOMERSET THERAPS LLC
At a glance
Sep 18, 2025
Approved
Generic (ANDA)
Application
AP
TE code
None
Listed patents
Key dates
Approval
FDA approval date of this drug product.
Sep 18, 2025
9 mo ago
Today
Pharmaceutical detail
Active ingredient
SODIUM ACETATE
Strength
100MEQ/50ML (2MEQ/ML)
Dosage form
SOLUTION
Route
INTRAVENOUS
TE code
AP
Application
ANDA 219826
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 220274 · EXTROVIS
- 2026SODIUM ACETATEGeneric (ANDA)
ANDA 218469 · AMNEAL
- 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.
