Carbinoxamine Maleate

   
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Carbinoxamine Maleate


Drug - Carbinoxamine Maleate
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) - Carbinoxamine Maleate
Multiple ingredients are in alphabetical order.

Strength - 4MG
The potency of the active ingredient(s), Carbinoxamine Maleate. May repeat for multiple part products.

Applicant - MIKART
The firm name holding legal responsibility for Carbinoxamine Maleate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 040442
The FDA assigned number to Carbinoxamine Maleate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Carbinoxamine Maleate. 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 19, 2003
The date Carbinoxamine Maleate 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) - Yes
The pioneer or innovator of Carbinoxamine Maleate. 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 Carbinoxamine Maleate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mikart Inc
The full name of the firm holding legal responsibility for the new application of Carbinoxamine Maleate.

Carbinoxamine Maleate