Kanamycin Sulfate

   
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Kanamycin Sulfate


Drug - Kanamycin Sulfate
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) - Kanamycin Sulfate
Multiple ingredients are in alphabetical order.

Strength - EQ 500MG BASE/2ML
The potency of the active ingredient(s), Kanamycin Sulfate. May repeat for multiple part products.

Applicant - SOLOPAK
The firm name holding legal responsibility for Kanamycin Sulfate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 062605
The FDA assigned number to Kanamycin Sulfate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Kanamycin Sulfate. 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 - Feb 26, 1986
The date Kanamycin Sulfate 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 Kanamycin Sulfate. 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 Kanamycin Sulfate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Solopak Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Kanamycin Sulfate.

Kanamycin Sulfate