NDC 70069-048 – Sodium acetate anhydrous

Sodium Acetate Anhydrous 164 mg/mL · Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC70069-048

Product details

Brand name
Sodium acetate anhydrous
Generic name
Sodium acetate anhydrous
Labeler
Somerset Therapeutics, LLC
Dosage form
Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA219826
Marketed since
October 23, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Sodium acetate anhydrous →

Package NDC codes (1)

Package NDCDescriptionSince
70069-048-2020 VIAL, GLASS in 1 CARTON (70069-048-20) / 100 mL in 1 VIAL, GLASSOct 23, 2025

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