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POTASSIUM CHLORIDE - 0264-1940-20 - (POTASSIUM CHLORIDE)

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Drug Information of POTASSIUM CHLORIDE

Product NDC: 0264-1940
Proprietary Name: POTASSIUM CHLORIDE
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 14.9    g/100mL & nbsp;   POTASSIUM CHLORIDE
Administration Route(s): PARENTERAL
Dosage Form(s): INJECTION, SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of POTASSIUM CHLORIDE

Product NDC: 0264-1940
Labeler Name: B. Braun Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA085870
Marketing Category: ANDA
Start Marketing Date: 19780321

Package Information of POTASSIUM CHLORIDE

Package NDC: 0264-1940-20
Package Description: 12 CONTAINER in 1 CASE (0264-1940-20) > 250 mL in 1 CONTAINER

NDC Information of POTASSIUM CHLORIDE

NDC Code 0264-1940-20
Proprietary Name POTASSIUM CHLORIDE
Package Description 12 CONTAINER in 1 CASE (0264-1940-20) > 250 mL in 1 CONTAINER
Product NDC 0264-1940
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name INJECTION, SOLUTION, CONCENTRATE
Route Name PARENTERAL
Start Marketing Date 19780321
Marketing Category Name ANDA
Labeler Name B. Braun Medical Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 14.9
Strength Unit g/100mL
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of POTASSIUM CHLORIDE


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