Clonidine Hcl


Clonidine Hcl

Drug - Clonidine 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) - Clonidine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 0.2MG
The potency of the active ingredient(s), Clonidine Hydrochloride. May repeat for multiple part products.

The firm name holding legal responsibility for Clonidine Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 072139
The FDA assigned number to Clonidine Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Clonidine 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 - Jun 13, 1988
The date Clonidine 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 Clonidine 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 Clonidine Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Warner Chilcott Div Warner Lambert Co
The full name of the firm holding legal responsibility for the new application of Clonidine Hcl.

Clonidine Hcl