Urocit-k

   
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Urocit-k


Drug - Urocit-k
The trade name of the product as shown on the labeling.

Dosage - TABLET, EXTENDED RELEASE; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Potassium Citrate
Multiple ingredients are in alphabetical order.

Strength - 10MEQ
The potency of the active ingredient(s), Potassium Citrate. May repeat for multiple part products.

Applicant - MISSION PHARMA
The firm name holding legal responsibility for Urocit-k. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019071
The FDA assigned number to Urocit-k. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Urocit-k. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Aug 31, 1992
The date Urocit-k was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".

Reference Listed Drug (RLD) - Yes
The pioneer or innovator of Urocit-k. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - RX
The group or category of approved drugs Urocit-k is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mission Pharmacal Co
The full name of the firm holding legal responsibility for the new application of Urocit-k.

Urocit-k


Tham-e 370mg/vial;1.75gm/vial;36gm/vial Injectable; Injection
Potassium Citrate 10meq/packet For Solution; Oral
Potassium Citrate 20meq/packet For Solution; Oral
Urocit-k 10meq Tablet, Extended Release; Oral
Sodium Chloride 0.9% And Potassium Chloride 0.15% In Plastic Container 150mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.15% In Plastic Container 150mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.22% In Plastic Container 220mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.224% 224mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container 300mg/100ml;900mg/100ml Injectable; Injection
Sodium Chloride 0.9% And Potassium Chloride 0.3% In Plastic Container 300mg/100ml;900mg/100ml Injectable; Injection

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