Dyclone

   
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Dyclone


Drug - Dyclone
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) - Dyclonine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 1% **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
The potency of the active ingredient(s), Dyclonine Hydrochloride. May repeat for multiple part products.

Applicant - ASTRAZENECA
The firm name holding legal responsibility for Dyclone. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 009925
The FDA assigned number to Dyclone. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Dyclone. 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 Dyclone 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 Dyclone. 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 Dyclone is in. Format is RX, OTC, DISCN.

Applicant Full Name - Astrazeneca Lp
The full name of the firm holding legal responsibility for the new application of Dyclone.

Dyclone