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Potassium Chloride - 0409-7075-14 - (POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride

Product NDC: 0409-7075
Proprietary Name: Potassium Chloride
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 200    meq/1000mL & nbsp;   POTASSIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 0409-7075
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA020161
Marketing Category: ANDA
Start Marketing Date: 20110401

Package Information of Potassium Chloride

Package NDC: 0409-7075-14
Package Description: 24 POUCH in 1 CASE (0409-7075-14) > 1 BAG in 1 POUCH > 50 mL in 1 BAG

NDC Information of Potassium Chloride

NDC Code 0409-7075-14
Proprietary Name Potassium Chloride
Package Description 24 POUCH in 1 CASE (0409-7075-14) > 1 BAG in 1 POUCH > 50 mL in 1 BAG
Product NDC 0409-7075
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20110401
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 200
Strength Unit meq/1000mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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