Loprox

   
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Loprox


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

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

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

Strength - 1%
The potency of the active ingredient(s), Ciclopirox. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 021159
The FDA assigned number to Loprox. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Loprox. 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 - Feb 28, 2003
The date Loprox 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 Loprox. 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 Loprox is in. Format is RX, OTC, DISCN.

Applicant Full Name - Medicis Pharmaceutical Corp
The full name of the firm holding legal responsibility for the new application of Loprox.

Loprox