urocit-k - 0178-0610-01 - (potassium citrate)

Alphabetical Index


Drug Information of urocit-k

Product NDC: 0178-0610
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: 0178-0610
Labeler Name: Mission Pharmacal Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019071
Marketing Category: NDA
Start Marketing Date: 19920901

Package Information of urocit-k

Package NDC: 0178-0610-01
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0610-01)

NDC Information of urocit-k

NDC Code 0178-0610-01
Proprietary Name urocit-k
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0178-0610-01)
Product NDC 0178-0610
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name potassium citrate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19920901
Marketing Category Name NDA
Labeler Name Mission Pharmacal Company
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