Ceftin

   
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Ceftin


Drug - Ceftin
The trade name of the product as shown on the labeling.

Dosage - TABLET; ORAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Cefuroxime Axetil
Multiple ingredients are in alphabetical order.

Strength - EQ 125MG BASE
The potency of the active ingredient(s), Cefuroxime Axetil. May repeat for multiple part products.

Applicant - GLAXOSMITHKLINE
The firm name holding legal responsibility for Ceftin. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 050605
The FDA assigned number to Ceftin. Format is nnnnnn.

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

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

Approval Date - Dec 28, 1987
The date Ceftin 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 Ceftin. 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 Ceftin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Glaxosmithkline
The full name of the firm holding legal responsibility for the new application of Ceftin.

Ceftin