Home > National Drug Code (NDC) > Potassium Chloride

Potassium Chloride - 49349-706-02 - (Potassium Chloride)

Alphabetical Index


Drug Information of Potassium Chloride

Product NDC: 49349-706
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: 49349-706
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019123
Marketing Category: NDA
Start Marketing Date: 20120911

Package Information of Potassium Chloride

Package NDC: 49349-706-02
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49349-706-02)

NDC Information of Potassium Chloride

NDC Code 49349-706-02
Proprietary Name Potassium Chloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (49349-706-02)
Product NDC 49349-706
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 20120911
Marketing Category Name NDA
Labeler Name REMEDYREPACK 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