Chlordiazepoxide Hcl


Chlordiazepoxide Hcl

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

The product dosage form and route separated by a semi-colon.

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

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

Applicant - IMPAX LABS
The firm name holding legal responsibility for Chlordiazepoxide Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 086212
The FDA assigned number to Chlordiazepoxide Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Chlordiazepoxide 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 - Approved Prior to Jan 1, 1982
The date Chlordiazepoxide 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 Chlordiazepoxide 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 Chlordiazepoxide Hcl is in. Format is RX, OTC, DISCN.

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

Chlordiazepoxide Hcl