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Sodium Acetate - 0409-3299-26 - (SODIUM ACETATE)

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Drug Information of Sodium Acetate

Product NDC: 0409-3299
Proprietary Name: Sodium Acetate
Non Proprietary Name: SODIUM ACETATE
Active Ingredient(s): 164    mg/mL & nbsp;   SODIUM ACETATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Acetate

Product NDC: 0409-3299
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20050430

Package Information of Sodium Acetate

Package NDC: 0409-3299-26
Package Description: 25 VIAL in 1 TRAY (0409-3299-26) > 50 mL in 1 VIAL

NDC Information of Sodium Acetate

NDC Code 0409-3299-26
Proprietary Name Sodium Acetate
Package Description 25 VIAL in 1 TRAY (0409-3299-26) > 50 mL in 1 VIAL
Product NDC 0409-3299
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM ACETATE
Dosage Form Name SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20050430
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Hospira, Inc.
Substance Name SODIUM ACETATE ANHYDROUS
Strength Number 164
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Sodium Acetate


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