K-Tab - 0074-7804-13 - (Potassium Chloride)

Alphabetical Index


Drug Information of K-Tab

Product NDC: 0074-7804
Proprietary Name: K-Tab
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 K-Tab

Product NDC: 0074-7804
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018279
Marketing Category: NDA
Start Marketing Date: 19800609

Package Information of K-Tab

Package NDC: 0074-7804-13
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-7804-13)

NDC Information of K-Tab

NDC Code 0074-7804-13
Proprietary Name K-Tab
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0074-7804-13)
Product NDC 0074-7804
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 19800609
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name POTASSIUM CHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of K-Tab


General Information