Desogestrel And Ethinyl Estradiol

   
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Desogestrel And Ethinyl Estradiol


Drug - Desogestrel And Ethinyl Estradiol
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL-28
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Desogestrel; Ethinyl Estradiol
Multiple ingredients are in alphabetical order.

Strength - 0.15MG;0.03MG
The potency of the active ingredient(s), Desogestrel; Ethinyl Estradiol. May repeat for multiple part products.

Applicant - WATSON LABS
The firm name holding legal responsibility for Desogestrel And Ethinyl Estradiol. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076915
The FDA assigned number to Desogestrel And Ethinyl Estradiol. Format is nnnnnn.

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

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

Approval Date - Jul 29, 2005
The date Desogestrel And Ethinyl Estradiol 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 Desogestrel And Ethinyl Estradiol. 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 Desogestrel And Ethinyl Estradiol is in. Format is RX, OTC, DISCN.

Applicant Full Name - Watson Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Desogestrel And Ethinyl Estradiol.

Desogestrel And Ethinyl Estradiol