Condylox

   
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Condylox


Drug - Condylox
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) - Podofilox
Multiple ingredients are in alphabetical order.

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

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

New Drug Application (NDA) Number - 019795
The FDA assigned number to Condylox. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Condylox. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - Dec 13, 1990
The date Condylox 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 Condylox. 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 Condylox is in. Format is RX, OTC, DISCN.

Applicant Full Name - Oclassen Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Condylox.

Condylox