Strattera

   
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Strattera


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

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

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

Strength - 25MG
The potency of the active ingredient(s), Atomoxetine Hydrochloride. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 021411
The FDA assigned number to Strattera. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Strattera. 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 - Nov 26, 2002
The date Strattera 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 Strattera. 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 Strattera is in. Format is RX, OTC, DISCN.

Applicant Full Name - Eli Lilly And Co
The full name of the firm holding legal responsibility for the new application of Strattera.

Strattera