Muse

   
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Muse


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

Dosage - SUPPOSITORY; URETHRAL
The product dosage form and route separated by a semi-colon.

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

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

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

New Drug Application (NDA) Number - 020700
The FDA assigned number to Muse. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Muse. 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 19, 1996
The date Muse 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 Muse. 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 Muse is in. Format is RX, OTC, DISCN.

Applicant Full Name - Vivus Inc
The full name of the firm holding legal responsibility for the new application of Muse.

Muse