Ceftriaxone And Dextrose In Duplex Container

   
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Ceftriaxone And Dextrose In Duplex Container


Drug - Ceftriaxone And Dextrose In Duplex Container
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) - Ceftriaxone Sodium
Multiple ingredients are in alphabetical order.

Strength - EQ 2GM BASE/VIAL
The potency of the active ingredient(s), Ceftriaxone Sodium. May repeat for multiple part products.

Applicant - B BRAUN
The firm name holding legal responsibility for Ceftriaxone And Dextrose In Duplex Container. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 050796
The FDA assigned number to Ceftriaxone And Dextrose In Duplex Container. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Ceftriaxone And Dextrose In Duplex Container. 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 - Apr 20, 2005
The date Ceftriaxone And Dextrose In Duplex Container 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) - Yes
The pioneer or innovator of Ceftriaxone And Dextrose In Duplex Container. 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 Ceftriaxone And Dextrose In Duplex Container is in. Format is RX, OTC, DISCN.

Applicant Full Name - B Braun Medical Inc
The full name of the firm holding legal responsibility for the new application of Ceftriaxone And Dextrose In Duplex Container.

Ceftriaxone And Dextrose In Duplex Container