Dimethyl Sulfoxide

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Dimethyl Sulfoxide

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

The product dosage form and route separated by a semi-colon.

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

Strength - 50%
The potency of the active ingredient(s), Dimethyl Sulfoxide. May repeat for multiple part products.

The firm name holding legal responsibility for Dimethyl Sulfoxide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 076185
The FDA assigned number to Dimethyl Sulfoxide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Dimethyl Sulfoxide. 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 - Nov 29, 2002
The date Dimethyl Sulfoxide 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 Dimethyl Sulfoxide. 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 Dimethyl Sulfoxide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bioniche Pharma (canada) Ltd
The full name of the firm holding legal responsibility for the new application of Dimethyl Sulfoxide.

Dimethyl Sulfoxide