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Potassium Acetate - 0517-5024-25 - (Potassium Acetate)

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Drug Information of Potassium Acetate

Product NDC: 0517-5024
Proprietary Name: Potassium Acetate
Non Proprietary Name: Potassium Acetate
Active Ingredient(s): 392    mg/mL & nbsp;   Potassium Acetate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Acetate

Product NDC: 0517-5024
Labeler Name: American Regent, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19900930

Package Information of Potassium Acetate

Package NDC: 0517-5024-25
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5024-25) > 50 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Potassium Acetate

NDC Code 0517-5024-25
Proprietary Name Potassium Acetate
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5024-25) > 50 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0517-5024
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Acetate
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 19900930
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name American Regent, Inc.
Substance Name POTASSIUM ACETATE
Strength Number 392
Strength Unit mg/mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Acetate


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