Nuromax

   
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Nuromax


Drug - Nuromax
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) - Doxacurium Chloride
Multiple ingredients are in alphabetical order.

Strength - EQ 1MG BASE/ML
The potency of the active ingredient(s), Doxacurium Chloride. May repeat for multiple part products.

Applicant - ABBOTT
The firm name holding legal responsibility for Nuromax. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019946
The FDA assigned number to Nuromax. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Nuromax. 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 - Mar 7, 1991
The date Nuromax 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 Nuromax. 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 Nuromax is in. Format is RX, OTC, DISCN.

Applicant Full Name - Abbott Laboratories
The full name of the firm holding legal responsibility for the new application of Nuromax.

Nuromax