Home > National Drug Code (NDC) > Sodium Acetate

Sodium Acetate - 0409-7299-73 - (SODIUM ACETATE)

Alphabetical Index


Drug Information of Sodium Acetate

Product NDC: 0409-7299
Proprietary Name: Sodium Acetate
Non Proprietary Name: SODIUM ACETATE
Active Ingredient(s): 3.28    g/20mL & nbsp;   SODIUM ACETATE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Sodium Acetate

Product NDC: 0409-7299
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018893
Marketing Category: NDA
Start Marketing Date: 20110823

Package Information of Sodium Acetate

Package NDC: 0409-7299-73
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73) > 20 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Sodium Acetate

NDC Code 0409-7299-73
Proprietary Name Sodium Acetate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-7299
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM ACETATE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20110823
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name SODIUM ACETATE
Strength Number 3.28
Strength Unit g/20mL
Pharmaceutical Classes

Complete Information of Sodium Acetate


General Information