Clonidine Hcl And Chlorthalidone

   
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Clonidine Hcl And Chlorthalidone


Drug - Clonidine Hcl And Chlorthalidone
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) - Chlorthalidone; Clonidine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 15MG;0.3MG
The potency of the active ingredient(s), Chlorthalidone; Clonidine Hydrochloride. May repeat for multiple part products.

Applicant - PAR PHARM
The firm name holding legal responsibility for Clonidine Hcl And Chlorthalidone. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 071142
The FDA assigned number to Clonidine Hcl And Chlorthalidone. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Clonidine Hcl And Chlorthalidone. 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 - Dec 16, 1987
The date Clonidine Hcl And Chlorthalidone 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 And Chlorthalidone. 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 And Chlorthalidone is in. Format is RX, OTC, DISCN.

Applicant Full Name - Par Pharmaceutical Inc
The full name of the firm holding legal responsibility for the new application of Clonidine Hcl And Chlorthalidone.

Clonidine Hcl And Chlorthalidone