Thioridazine Hcl Intensol

   
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Thioridazine Hcl Intensol


Drug - Thioridazine Hcl Intensol
The trade name of the product as shown on the labeling.

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

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

Strength - 30MG/ML
The potency of the active ingredient(s), Thioridazine Hydrochloride. May repeat for multiple part products.

Applicant - ROXANE
The firm name holding legal responsibility for Thioridazine Hcl Intensol. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088941
The FDA assigned number to Thioridazine Hcl Intensol. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Thioridazine Hcl Intensol. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

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

Approval Date - Dec 16, 1985
The date Thioridazine Hcl Intensol 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 Thioridazine Hcl Intensol. 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 Thioridazine Hcl Intensol is in. Format is RX, OTC, DISCN.

Applicant Full Name - Roxane Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Thioridazine Hcl Intensol.

Thioridazine Hcl Intensol