Extra-strength Aim

   
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Extra-strength Aim


Drug - Extra-strength Aim
The trade name of the product as shown on the labeling.

Dosage - GEL; DENTAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Sodium Monofluorophosphate
Multiple ingredients are in alphabetical order.

Strength - 1.2%
The potency of the active ingredient(s), Sodium Monofluorophosphate. May repeat for multiple part products.

Applicant - CHESEBROUGH PONDS
The firm name holding legal responsibility for Extra-strength Aim. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019518
The FDA assigned number to Extra-strength Aim. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Extra-strength Aim. 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 6, 1986
The date Extra-strength Aim 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 Extra-strength Aim. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - OTC
The group or category of approved drugs Extra-strength Aim is in. Format is RX, OTC, DISCN.

Applicant Full Name - Chesebrough Ponds Inc
The full name of the firm holding legal responsibility for the new application of Extra-strength Aim.

Extra-strength Aim