Succinylcholine Chloride

   
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Succinylcholine Chloride


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

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

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

Strength - 20MG/ML
The potency of the active ingredient(s), Succinylcholine Chloride. May repeat for multiple part products.

Applicant - ORGANON USA INC
The firm name holding legal responsibility for Succinylcholine Chloride. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 080997
The FDA assigned number to Succinylcholine Chloride. Format is nnnnnn.

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

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

Approval Date - Approved Prior to Jan 1, 1982
The date Succinylcholine Chloride 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 Succinylcholine Chloride. 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 Succinylcholine Chloride is in. Format is RX, OTC, DISCN.

Applicant Full Name - Organon Usa Inc
The full name of the firm holding legal responsibility for the new application of Succinylcholine Chloride.

Succinylcholine Chloride