Sodium Thiosulfate

   
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Sodium Thiosulfate


Drug - Sodium Thiosulfate
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) - Sodium Thiosulfate
Multiple ingredients are in alphabetical order.

Strength - 250MG/ML
The potency of the active ingredient(s), Sodium Thiosulfate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 020166
The FDA assigned number to Sodium Thiosulfate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Sodium Thiosulfate. 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 - Feb 14, 1992
The date Sodium Thiosulfate 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 Sodium Thiosulfate. 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 Sodium Thiosulfate is in. Format is RX, OTC, DISCN.

Applicant Full Name - United States Army Office Surgeon General
The full name of the firm holding legal responsibility for the new application of Sodium Thiosulfate.

Sodium Thiosulfate