Fenoldopam Mesylate

   
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Fenoldopam Mesylate


Drug - Fenoldopam Mesylate
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Fenoldopam Mesylate
Multiple ingredients are in alphabetical order.

Strength - EQ 10MG BASE/ML
The potency of the active ingredient(s), Fenoldopam Mesylate. May repeat for multiple part products.

Applicant - BEDFORD LABS
The firm name holding legal responsibility for Fenoldopam Mesylate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076582
The FDA assigned number to Fenoldopam Mesylate. Format is nnnnnn.

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

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

Approval Date - Oct 12, 2004
The date Fenoldopam Mesylate 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 Fenoldopam Mesylate. 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 Fenoldopam Mesylate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bedford Laboratories
The full name of the firm holding legal responsibility for the new application of Fenoldopam Mesylate.

Fenoldopam Mesylate