Isoflurane

   
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Isoflurane


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

Dosage - LIQUID; INHALATION
The product dosage form and route separated by a semi-colon.

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

Strength - 99.9%
The potency of the active ingredient(s), Isoflurane. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 074416
The FDA assigned number to Isoflurane. Format is nnnnnn.

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

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

Approval Date - Sep 30, 1994
The date Isoflurane 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 Isoflurane. 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 Isoflurane is in. Format is RX, OTC, DISCN.

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

Isoflurane