Ten-k
Drug - Ten-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 Chloride
Multiple ingredients are in alphabetical order.
Strength -
10MEQ
The potency of the active ingredient(s), Potassium Chloride. May repeat for multiple part products.
Applicant -
NOVARTIS
The firm name holding legal responsibility for Ten-k. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
019381
The FDA assigned number to Ten-k. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Ten-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 -
Apr 16, 1986
The date Ten-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) -
No
The pioneer or innovator of Ten-k. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
DISCN
The group or category of approved drugs Ten-k is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Novartis Pharmaceuticals Corp
The full name of the firm holding legal responsibility for the new application of Ten-k.
Ten-k
Potassium Chloride 20meq Tablet, Extended Release; Oral Potassium Chloride 20meq Tablet, Extended Release; Oral Slow-k 8meq Tablet, Extended Release; Oral Ten-k 10meq Tablet, Extended Release; Oral Klotrix 10meq Tablet, Extended Release; Oral K-tab 10meq Tablet, Extended Release; Oral Potassium Chloride 8meq Tablet, Extended Release; Oral Potassium Chloride 10meq Tablet, Extended Release; Oral Potassium Chloride 20meq Tablet, Extended Release; Oral Potassium Chloride 8meq Tablet, Extended Release; Oral
NewDrugInformation
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