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Potassium Chloride - 63323-965-10 - (POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride

Product NDC: 63323-965
Proprietary Name: Potassium Chloride
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 2    meq/mL & nbsp;   POTASSIUM CHLORIDE
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 63323-965
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088901
Marketing Category: ANDA
Start Marketing Date: 19990927

Package Information of Potassium Chloride

Package NDC: 63323-965-10
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-965-10) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Potassium Chloride

NDC Code 63323-965-10
Proprietary Name Potassium Chloride
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-965-10) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-965
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 19990927
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name POTASSIUM CHLORIDE
Strength Number 2
Strength Unit meq/mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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