Sus-phrine Sulfite-free

   
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Sus-phrine Sulfite-free


Drug - Sus-phrine Sulfite-free
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) - Epinephrine
Multiple ingredients are in alphabetical order.

Strength - 1.5MG/AMP
The potency of the active ingredient(s), Epinephrine. May repeat for multiple part products.

Applicant - FOREST LABS
The firm name holding legal responsibility for Sus-phrine Sulfite-free. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 007942
The FDA assigned number to Sus-phrine Sulfite-free. Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Sus-phrine Sulfite-free. 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 - Feb 5, 1999
The date Sus-phrine Sulfite-free 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 Sus-phrine Sulfite-free. 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 Sus-phrine Sulfite-free is in. Format is RX, OTC, DISCN.

Applicant Full Name - Forest Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Sus-phrine Sulfite-free.

Sus-phrine Sulfite-free