Miostat

   
Google
 
Web NewDrugInformation.com

Miostat


Drug - Miostat
The trade name of the product as shown on the labeling.

Dosage - SOLUTION; INTRAOCULAR
The product dosage form and route separated by a semi-colon.

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

Strength - 0.01%
The potency of the active ingredient(s), Carbachol. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 016968
The FDA assigned number to Miostat. Format is nnnnnn.

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

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

Approval Date - Approved Prior to Jan 1, 1982
The date Miostat 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 Miostat. 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 Miostat is in. Format is RX, OTC, DISCN.

Applicant Full Name - Alcon Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Miostat.

Miostat