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Potassium Acetate - 0409-3294-51 - (POTASSIUM ACETATE)

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Drug Information of Potassium Acetate

Product NDC: 0409-3294
Proprietary Name: Potassium Acetate
Non Proprietary Name: POTASSIUM ACETATE
Active Ingredient(s): 196.3    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: 0409-3294
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018896
Marketing Category: NDA
Start Marketing Date: 20100408

Package Information of Potassium Acetate

Package NDC: 0409-3294-51
Package Description: 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0409-3294-51) > 50 mL in 1 VIAL, PHARMACY BULK PACKAGE

NDC Information of Potassium Acetate

NDC Code 0409-3294-51
Proprietary Name Potassium Acetate
Package Description 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (0409-3294-51) > 50 mL in 1 VIAL, PHARMACY BULK PACKAGE
Product NDC 0409-3294
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM ACETATE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20100408
Marketing Category Name NDA
Labeler Name Hospira, Inc.
Substance Name POTASSIUM ACETATE
Strength Number 196.3
Strength Unit mg/mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Acetate


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