Chlorpromazine Hcl

   
Google
 
Web NewDrugInformation.com

Chlorpromazine Hcl


Drug - Chlorpromazine Hcl
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) - Chlorpromazine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 10MG
The potency of the active ingredient(s), Chlorpromazine Hydrochloride. May repeat for multiple part products.

Applicant - WEST WARD
The firm name holding legal responsibility for Chlorpromazine Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 087783
The FDA assigned number to Chlorpromazine Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Chlorpromazine Hcl. 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 16, 1982
The date Chlorpromazine Hcl 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 Chlorpromazine Hcl. 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 Chlorpromazine Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - West Ward Pharmaceutical Corp
The full name of the firm holding legal responsibility for the new application of Chlorpromazine Hcl.

Chlorpromazine Hcl