Sular

   
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Sular


Drug - Sular
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) - Nisoldipine
Multiple ingredients are in alphabetical order.

Strength - 10MG
The potency of the active ingredient(s), Nisoldipine. May repeat for multiple part products.

Applicant - FIRST HORIZON
The firm name holding legal responsibility for Sular. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 020356
The FDA assigned number to Sular. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Sular. 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 - Feb 2, 1995
The date Sular 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 Sular. 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 Sular is in. Format is RX, OTC, DISCN.

Applicant Full Name - First Horizon Pharmaceutical Corp
The full name of the firm holding legal responsibility for the new application of Sular.

Sular