Daypro Alta

   
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Daypro Alta


Drug - Daypro Alta
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) - Oxaprozin Potassium
Multiple ingredients are in alphabetical order.

Strength - 600MG
The potency of the active ingredient(s), Oxaprozin Potassium. May repeat for multiple part products.

Applicant - GD SEARLE
The firm name holding legal responsibility for Daypro Alta. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020776
The FDA assigned number to Daypro Alta. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Daypro Alta. 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 17, 2002
The date Daypro Alta 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 Daypro Alta. 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 Daypro Alta is in. Format is RX, OTC, DISCN.

Applicant Full Name - Gd Searle Llc
The full name of the firm holding legal responsibility for the new application of Daypro Alta.

Daypro Alta