Technelite

   
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Technelite


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

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

Active Ingredient(s) - Technetium Tc-99m Sodium Pertechnetate Generator
Multiple ingredients are in alphabetical order.

Strength - 0.0083-2.7 CI/GENERATOR
The potency of the active ingredient(s), Technetium Tc-99m Sodium Pertechnetate Generator. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 017771
The FDA assigned number to Technelite. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Technelite. 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 Technelite 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 Technelite. 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 Technelite 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 Technelite.

Technelite