Hydroxyzine Pamoate

   
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Hydroxyzine Pamoate


Drug - Hydroxyzine Pamoate
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Hydroxyzine Pamoate
Multiple ingredients are in alphabetical order.

Strength - EQ 100MG HCL
The potency of the active ingredient(s), Hydroxyzine Pamoate. May repeat for multiple part products.

Applicant - BARR
The firm name holding legal responsibility for Hydroxyzine Pamoate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088488
The FDA assigned number to Hydroxyzine Pamoate. Format is nnnnnn.

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

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

Approval Date - Jun 15, 1984
The date Hydroxyzine Pamoate 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 Hydroxyzine Pamoate. 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 Hydroxyzine Pamoate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Barr Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Hydroxyzine Pamoate.

Hydroxyzine Pamoate