Seconal Sodium

   
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Seconal Sodium


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

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

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

Strength - 200MG
The potency of the active ingredient(s), Secobarbital Sodium. May repeat for multiple part products.

Applicant - LILLY
The firm name holding legal responsibility for Seconal Sodium. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 086530
The FDA assigned number to Seconal Sodium. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Seconal Sodium. 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 Seconal Sodium 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 Seconal Sodium. 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 Seconal Sodium is in. Format is RX, OTC, DISCN.

Applicant Full Name - Eli Lilly And Co
The full name of the firm holding legal responsibility for the new application of Seconal Sodium.

Seconal Sodium