Cefazolin

   
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Cefazolin


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

Strength - EQ 1GM BASE
The potency of the active ingredient(s), Cefazolin Sodium. May repeat for multiple part products.

Applicant - ORCHID HLTHCARE
The firm name holding legal responsibility for Cefazolin. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 065244
The FDA assigned number to Cefazolin. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Cefazolin. 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 12, 2005
The date Cefazolin 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 Cefazolin. 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 Cefazolin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Orchid Healthcare
The full name of the firm holding legal responsibility for the new application of Cefazolin.

Cefazolin