NDC 70069-047 – Sodium acetate anhydrous

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

Human Prescription Drug

Product NDC70069-047

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
70069-047-2525 VIAL, GLASS in 1 CARTON (70069-047-25) / 50 mL in 1 VIAL, GLASSOct 23, 2025

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