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Potassium Chloride in Dextrose - 0338-0685-04 - (Potassium Chloride and Dextrose Monohydrate)

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Drug Information of Potassium Chloride in Dextrose

Product NDC: 0338-0685
Proprietary Name: Potassium Chloride in Dextrose
Non Proprietary Name: Potassium Chloride and Dextrose Monohydrate
Active Ingredient(s): 5; 224    g/100mL; mg/100mL & nbsp;   Potassium Chloride and Dextrose Monohydrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride in Dextrose

Product NDC: 0338-0685
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017634
Marketing Category: NDA
Start Marketing Date: 19790201

Package Information of Potassium Chloride in Dextrose

Package NDC: 0338-0685-04
Package Description: 1000 mL in 1 BAG (0338-0685-04)

NDC Information of Potassium Chloride in Dextrose

NDC Code 0338-0685-04
Proprietary Name Potassium Chloride in Dextrose
Package Description 1000 mL in 1 BAG (0338-0685-04)
Product NDC 0338-0685
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride and Dextrose Monohydrate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19790201
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name DEXTROSE MONOHYDRATE; POTASSIUM CHLORIDE
Strength Number 5; 224
Strength Unit g/100mL; mg/100mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride in Dextrose


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