UROCIT-K - 54868-4779-2 - (potassium citrate)

Alphabetical Index


Drug Information of UROCIT-K

Product NDC: 54868-4779
Proprietary Name: UROCIT-K
Non Proprietary Name: potassium citrate
Active Ingredient(s): 10    meq/1 & nbsp;   potassium citrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of UROCIT-K

Product NDC: 54868-4779
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019071
Marketing Category: NDA
Start Marketing Date: 20030417

Package Information of UROCIT-K

Package NDC: 54868-4779-2
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4779-2)

NDC Information of UROCIT-K

NDC Code 54868-4779-2
Proprietary Name UROCIT-K
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4779-2)
Product NDC 54868-4779
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium citrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030417
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name POTASSIUM CITRATE
Strength Number 10
Strength Unit meq/1
Pharmaceutical Classes Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC]

Complete Information of UROCIT-K


General Information