Doxycycline Hyclate

   
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Doxycycline Hyclate


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

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

Active Ingredient(s) - Doxycycline Hyclate
Multiple ingredients are in alphabetical order.

Strength - EQ 100MG BASE
The potency of the active ingredient(s), Doxycycline Hyclate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 061717
The FDA assigned number to Doxycycline Hyclate. Format is nnnnnn.

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

Applicant Full Name - Watson Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Doxycycline Hyclate.

Doxycycline Hyclate