Dyna-hex

   
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Dyna-hex


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

Dosage - SOLUTION; TOPICAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Chlorhexidine Gluconate
Multiple ingredients are in alphabetical order.

Strength - 0.75%
The potency of the active ingredient(s), Chlorhexidine Gluconate. May repeat for multiple part products.

Applicant - XTTRIUM
The firm name holding legal responsibility for Dyna-hex. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020111
The FDA assigned number to Dyna-hex. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Dyna-hex. 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 - Sep 11, 1997
The date Dyna-hex 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 Dyna-hex. 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 Dyna-hex is in. Format is RX, OTC, DISCN.

Applicant Full Name - Xttrium Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Dyna-hex.

Dyna-hex