Monoket

   
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Monoket


Drug - Monoket
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) - Isosorbide Mononitrate
Multiple ingredients are in alphabetical order.

Strength - 20MG
The potency of the active ingredient(s), Isosorbide Mononitrate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 020215
The FDA assigned number to Monoket. Format is nnnnnn.

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

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

Approval Date - Jun 30, 1993
The date Monoket 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 Monoket. 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 Monoket is in. Format is RX, OTC, DISCN.

Applicant Full Name - Schwarz Gmbh
The full name of the firm holding legal responsibility for the new application of Monoket.

Monoket