Cogentin

   
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Cogentin


Drug - Cogentin
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) - Benztropine Mesylate
Multiple ingredients are in alphabetical order.

Strength - 0.5MG
The potency of the active ingredient(s), Benztropine Mesylate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 009193
The FDA assigned number to Cogentin. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Cogentin. 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 - Approved Prior to Jan 1, 1982
The date Cogentin 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 Cogentin. 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 Cogentin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Merck And Co Inc
The full name of the firm holding legal responsibility for the new application of Cogentin.

Cogentin