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POTASSIUM CHLORIDE - 0409-6636-01 - (POTASSIUM CHLORIDE)

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Drug Information of POTASSIUM CHLORIDE

Product NDC: 0409-6636
Proprietary Name: POTASSIUM CHLORIDE
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 149    mg/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: 0409-6636
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080205
Marketing Category: ANDA
Start Marketing Date: 19720316

Package Information of POTASSIUM CHLORIDE

Package NDC: 0409-6636-01
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6636-01) > 5 mL in 1 VIAL, SINGLE-DOSE

NDC Information of POTASSIUM CHLORIDE

NDC Code 0409-6636-01
Proprietary Name POTASSIUM CHLORIDE
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6636-01) > 5 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0409-6636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 19720316
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 149
Strength Unit mg/mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of POTASSIUM CHLORIDE


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