Efidac 24 Chlorpheniramine Maleate

   
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Efidac 24 Chlorpheniramine Maleate


Drug - Efidac 24 Chlorpheniramine Maleate
The trade name of the product as shown on the labeling.

Dosage - TABLET, EXTENDED RELEASE; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Chlorpheniramine Maleate
Multiple ingredients are in alphabetical order.

Strength - 16MG
The potency of the active ingredient(s), Chlorpheniramine Maleate. May repeat for multiple part products.

Applicant - ALZA
The firm name holding legal responsibility for Efidac 24 Chlorpheniramine Maleate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 019746
The FDA assigned number to Efidac 24 Chlorpheniramine Maleate. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Efidac 24 Chlorpheniramine 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 - Nov 18, 1994
The date Efidac 24 Chlorpheniramine 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) - No
The pioneer or innovator of Efidac 24 Chlorpheniramine Maleate. 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 Efidac 24 Chlorpheniramine Maleate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Alza Corp
The full name of the firm holding legal responsibility for the new application of Efidac 24 Chlorpheniramine Maleate.

Efidac 24 Chlorpheniramine Maleate