NDC 0517-5023

Sodum Acetate

Sodium Acetate

Sodum Acetate is a Intravenous Injection, Solution, Concentrate in the Human Prescription Drug category. It is labeled and distributed by American Regent, Inc.. The primary component is Sodium Acetate Anhydrous.

• Product ID: 0517-5023_0954629f-ef6f-42d1-b3c9-409597fb8a24
• NDC: 0517-5023
• Product Type: Human Prescription Drug
• Proprietary Name: Sodum Acetate
• Generic Name: Sodium Acetate
• Dosage Form: Injection, Solution, Concentrate
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 1990-09-30
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: American Regent, Inc.
• Substance Name: SODIUM ACETATE ANHYDROUS
• Active Ingredient Strength: 328 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 0517-5023-25

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5023-25) > 50 mL in 1 VIAL, SINGLE-DOSE

• Marketing Start Date: 1990-09-30
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0517-5023-25 [00517502325]

Sodum Acetate INJECTION, SOLUTION, CONCENTRATE

• Marketing Category: UNAPPROVED DRUG OTHER
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 1990-09-30

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM ACETATE ANHYDROUS	328 mg/mL

OpenFDA Data

• SPL SET ID: b619ee23-26ca-48c8-be40-7911f575e43d
• Manufacturer:
  • American Regent, Inc.
• UNII:
  • NVG71ZZ7P0
• RxNorm Concept Unique ID - RxCUI:
  • 1859502

NDC Crossover Matching brand name "Sodum Acetate" or generic name "Sodium Acetate"

NDC	Brand Name	Generic Name
0517-5023	Sodum Acetate	Sodium Acetate
0409-3299	Sodium Acetate	sodium acetate
0409-7299	Sodium Acetate	SODIUM ACETATE
51754-9995	Sodium Acetate	Sodium Acetate
63323-032	SODIUM ACETATE	SODIUM ACETATE
69784-230	SODIUM ACETATE	SODIUM ACETATE
69784-231	SODIUM ACETATE	SODIUM ACETATE