Vecuronium Bromide

   
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Vecuronium Bromide


Drug - Vecuronium Bromide
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) - Vecuronium Bromide
Multiple ingredients are in alphabetical order.

Strength - 20MG/VIAL
The potency of the active ingredient(s), Vecuronium Bromide. May repeat for multiple part products.

Applicant - STERIS
The firm name holding legal responsibility for Vecuronium Bromide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 074334
The FDA assigned number to Vecuronium Bromide. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Vecuronium Bromide. 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 - Aug 31, 1995
The date Vecuronium Bromide 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 Vecuronium Bromide. 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 Vecuronium Bromide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Steris Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Vecuronium Bromide.

Vecuronium Bromide