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Potassium Chloride - 53808-0397-1 - (POTASSIUM CHLORIDE)

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Drug Information of Potassium Chloride

Product NDC: 53808-0397
Proprietary Name: Potassium Chloride
Non Proprietary Name: POTASSIUM CHLORIDE
Active Ingredient(s): 600    mg/1 & nbsp;   POTASSIUM CHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 53808-0397
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076368
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Potassium Chloride

Package NDC: 53808-0397-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (53808-0397-1)

NDC Information of Potassium Chloride

NDC Code 53808-0397-1
Proprietary Name Potassium Chloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (53808-0397-1)
Product NDC 53808-0397
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name POTASSIUM CHLORIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name POTASSIUM CHLORIDE
Strength Number 600
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


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