Apogen

   
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Apogen


Drug - Apogen
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) - Gentamicin Sulfate
Multiple ingredients are in alphabetical order.

Strength - EQ 40MG BASE/ML
The potency of the active ingredient(s), Gentamicin Sulfate. May repeat for multiple part products.

Applicant - KING PHARMS
The firm name holding legal responsibility for Apogen. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 062289
The FDA assigned number to Apogen. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Apogen. 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 - Approved Prior to Jan 1, 1982
The date Apogen 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 Apogen. 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 Apogen is in. Format is RX, OTC, DISCN.

Applicant Full Name - King Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Apogen.

Apogen