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Potassium Chloride - 0338-0707-48 - (POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride

Product NDC: 0338-0707
Proprietary Name: Potassium Chloride
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 300    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: 0338-0707
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019904
Marketing Category: NDA
Start Marketing Date: 19891226

Package Information of Potassium Chloride

Package NDC: 0338-0707-48
Package Description: 24 BAG in 1 CARTON (0338-0707-48) > 100 mL in 1 BAG

NDC Information of Potassium Chloride

NDC Code 0338-0707-48
Proprietary Name Potassium Chloride
Package Description 24 BAG in 1 CARTON (0338-0707-48) > 100 mL in 1 BAG
Product NDC 0338-0707
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19891226
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name POTASSIUM CHLORIDE
Strength Number 300
Strength Unit meq/1000mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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