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

The product dosage form and route separated by a semi-colon.

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

Strength - 6MG/24HR
The potency of the active ingredient(s), Testosterone. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 019762
The FDA assigned number to Testoderm. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Testoderm. 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 - Oct 12, 1993
The date Testoderm 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 Testoderm. 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 Testoderm is in. Format is RX, OTC, DISCN.

Applicant Full Name - Alza Corp
The full name of the firm holding legal responsibility for the new application of Testoderm.