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Potassium Chloride - 68382-600-01 - (Potassium Chloride)

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Drug Information of Potassium Chloride

Product NDC: 68382-600
Proprietary Name: Potassium Chloride
Non Proprietary Name: Potassium Chloride
Active Ingredient(s): 750    mg/1 & nbsp;   Potassium Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Potassium Chloride

Product NDC: 68382-600
Labeler Name: Zydus Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018279
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20110222

Package Information of Potassium Chloride

Package NDC: 68382-600-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-600-01)

NDC Information of Potassium Chloride

NDC Code 68382-600-01
Proprietary Name Potassium Chloride
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68382-600-01)
Product NDC 68382-600
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Potassium Chloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110222
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Zydus Pharmaceuticals USA Inc
Substance Name POTASSIUM CHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of Potassium Chloride


General Information