Doxycycline

   
Google
 
Web NewDrugInformation.com

Doxycycline


Drug - Doxycycline
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) - Doxycycline Hyclate
Multiple ingredients are in alphabetical order.

Strength - EQ 200MG BASE/VIAL
The potency of the active ingredient(s), Doxycycline Hyclate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 062569
The FDA assigned number to Doxycycline. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Doxycycline. 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 - Mar 9, 1988
The date Doxycycline 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 Doxycycline. 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 Doxycycline is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bedford Laboratories Div Ben Venue Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Doxycycline.

Doxycycline