Symadine

   
Google
 
Web NewDrugInformation.com

Symadine


Drug - Symadine
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) - Amantadine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 100MG
The potency of the active ingredient(s), Amantadine Hydrochloride. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 071000
The FDA assigned number to Symadine. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Symadine. 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 - Sep 4, 1986
The date Symadine 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 Symadine. 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 Symadine is in. Format is RX, OTC, DISCN.

Applicant Full Name - Solvay Pharmaceuticals
The full name of the firm holding legal responsibility for the new application of Symadine.

Symadine