Amerscan Mdp Kit

   
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Amerscan Mdp Kit


Drug - Amerscan Mdp Kit
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) - Technetium Tc-99m Medronate Kit
Multiple ingredients are in alphabetical order.

Strength - N/A
The potency of the active ingredient(s), Technetium Tc-99m Medronate Kit. May repeat for multiple part products.

Applicant - GE HEALTHCARE
The firm name holding legal responsibility for Amerscan Mdp Kit. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 018335
The FDA assigned number to Amerscan Mdp Kit. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Amerscan Mdp Kit. 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 - Aug 5, 1982
The date Amerscan Mdp Kit 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 Amerscan Mdp Kit. 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 Amerscan Mdp Kit is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ge Healthcare
The full name of the firm holding legal responsibility for the new application of Amerscan Mdp Kit.

Amerscan Mdp Kit