Thallous Chloride Tl 201

   
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Thallous Chloride Tl 201


Drug - Thallous Chloride Tl 201
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Thallous Chloride, Tl-201
Multiple ingredients are in alphabetical order.

Strength - 2mCi/ML
The potency of the active ingredient(s), Thallous Chloride, Tl-201. May repeat for multiple part products.

Applicant - BRISTOL MYERS SQUIBB
The firm name holding legal responsibility for Thallous Chloride Tl 201. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017806
The FDA assigned number to Thallous Chloride Tl 201. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Thallous Chloride Tl 201. 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 - Oct 9, 1998
The date Thallous Chloride Tl 201 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) - Yes
The pioneer or innovator of Thallous Chloride Tl 201. 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 Thallous Chloride Tl 201 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bristol Myers Squibb Medical Imaging
The full name of the firm holding legal responsibility for the new application of Thallous Chloride Tl 201.

Thallous Chloride Tl 201