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Potassium Chloride in Sodium Chloride - 0338-0691-04 - (Potassium Chloride and Sodium Chloride)

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Drug Information of Potassium Chloride in Sodium Chloride

Product NDC: 0338-0691
Proprietary Name: Potassium Chloride in Sodium Chloride
Non Proprietary Name: Potassium Chloride and Sodium Chloride
Active Ingredient(s): 150; 900    mg/100mL; mg/100mL & nbsp;   Potassium Chloride and Sodium Chloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride in Sodium Chloride

Product NDC: 0338-0691
Labeler Name: Baxter Healthcare Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017648
Marketing Category: NDA
Start Marketing Date: 19790202

Package Information of Potassium Chloride in Sodium Chloride

Package NDC: 0338-0691-04
Package Description: 1000 mL in 1 BAG (0338-0691-04)

NDC Information of Potassium Chloride in Sodium Chloride

NDC Code 0338-0691-04
Proprietary Name Potassium Chloride in Sodium Chloride
Package Description 1000 mL in 1 BAG (0338-0691-04)
Product NDC 0338-0691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride and Sodium Chloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19790202
Marketing Category Name NDA
Labeler Name Baxter Healthcare Corporation
Substance Name POTASSIUM CHLORIDE; SODIUM CHLORIDE
Strength Number 150; 900
Strength Unit mg/100mL; mg/100mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride in Sodium Chloride


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