Pentothal

   
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Pentothal


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

Dosage - SUSPENSION; RECTAL
The product dosage form and route separated by a semi-colon.

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

Strength - 400MG/GM
The potency of the active ingredient(s), Thiopental Sodium. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 011679
The FDA assigned number to Pentothal. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Pentothal. 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 - Approved Prior to Jan 1, 1982
The date Pentothal 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 Pentothal. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Pentothal is in. Format is RX, OTC, DISCN.

Applicant Full Name - Abbott Laboratories Hosp Products Div
The full name of the firm holding legal responsibility for the new application of Pentothal.

Pentothal