Permethrin
Drug - Permethrin
The trade name of the product as shown on the labeling.
Dosage -
LOTION; TOPICAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Permethrin
Multiple ingredients are in alphabetical order.
Strength -
1%
The potency of the active ingredient(s), Permethrin. May repeat for multiple part products.
Applicant -
ALPHARMA US PHARMS
The firm name holding legal responsibility for Permethrin. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
075014
The FDA assigned number to Permethrin. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Permethrin. 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 -
Mar 28, 2000
The date Permethrin 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 Permethrin. 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 Permethrin is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Alpharma Us Pharmaceuticals Division
The full name of the firm holding legal responsibility for the new application of Permethrin.
Permethrin
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