Micro-k 10

   
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Micro-k 10


Drug - Micro-k 10
The trade name of the product as shown on the labeling.

Dosage - CAPSULE, 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 - KV PHARM
The firm name holding legal responsibility for Micro-k 10. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018238
The FDA assigned number to Micro-k 10. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Micro-k 10. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - May 14, 1984
The date Micro-k 10 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 Micro-k 10. 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 Micro-k 10 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Kv Pharmaceutical Co
The full name of the firm holding legal responsibility for the new application of Micro-k 10.

Micro-k 10