Estradiol And Norgestimate

   
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Estradiol And Norgestimate


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

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

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

Strength - 1MG,1MG;N/A,0.09MG
The potency of the active ingredient(s), Estradiol; Norgestimate. May repeat for multiple part products.

Applicant - BARR
The firm name holding legal responsibility for Estradiol And Norgestimate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076812
The FDA assigned number to Estradiol And Norgestimate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Estradiol And Norgestimate. 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 - Apr 29, 2005
The date Estradiol And Norgestimate 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 Estradiol And Norgestimate. 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 Estradiol And Norgestimate is in. Format is RX, OTC, DISCN.

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

Estradiol And Norgestimate