Prazosin Hcl

   
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Prazosin Hcl


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

Strength - EQ 1MG BASE
The potency of the active ingredient(s), Prazosin Hydrochloride. May repeat for multiple part products.

Applicant - IVAX PHARMS
The firm name holding legal responsibility for Prazosin Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 071994
The FDA assigned number to Prazosin Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Prazosin Hcl. 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 - Sep 12, 1988
The date Prazosin 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 Prazosin Hcl. 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 Prazosin Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ivax Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Prazosin Hcl.

Prazosin Hcl