Circanol

   
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Circanol


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

Dosage - TABLET; SUBLINGUAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Ergoloid Mesylates
Multiple ingredients are in alphabetical order.

Strength - 0.5MG
The potency of the active ingredient(s), Ergoloid Mesylates. May repeat for multiple part products.

Applicant - 3M
The firm name holding legal responsibility for Circanol. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 084868
The FDA assigned number to Circanol. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Circanol. 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 - Approved Prior to Jan 1, 1982
The date Circanol 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 Circanol. 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 Circanol is in. Format is RX, OTC, DISCN.

Applicant Full Name - 3m Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Circanol.

Circanol