Foscarnet Sodium

   
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Foscarnet Sodium


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

Strength - 2.4GM/100ML
The potency of the active ingredient(s), Foscarnet Sodium. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 077174
The FDA assigned number to Foscarnet Sodium. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Foscarnet Sodium. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AP
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - May 31, 2005
The date Foscarnet Sodium 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 Foscarnet Sodium. 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 Foscarnet Sodium is in. Format is RX, OTC, DISCN.

Applicant Full Name - Pharmaforce Inc
The full name of the firm holding legal responsibility for the new application of Foscarnet Sodium.

Foscarnet Sodium