Ultra-technekow Fm

   
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Ultra-technekow Fm


Drug - Ultra-technekow Fm
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 - 0.25-3 CI/GENERATOR
The potency of the active ingredient(s), Technetium Tc-99m Sodium Pertechnetate Generator. May repeat for multiple part products.

Applicant - MALLINCKRODT
The firm name holding legal responsibility for Ultra-technekow Fm. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017243
The FDA assigned number to Ultra-technekow Fm. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Ultra-technekow Fm. 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 Ultra-technekow Fm 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 Ultra-technekow Fm. 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 Ultra-technekow Fm is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mallinckrodt Medical Inc
The full name of the firm holding legal responsibility for the new application of Ultra-technekow Fm.

Ultra-technekow Fm