Doxychel Hyclate

   
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Doxychel Hyclate


Drug - Doxychel Hyclate
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 100MG BASE/VIAL
The potency of the active ingredient(s), Doxycycline Hyclate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 061953
The FDA assigned number to Doxychel Hyclate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Doxychel Hyclate. 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 Doxychel 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 Doxychel Hyclate. 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 Doxychel Hyclate is in. Format is RX, OTC, DISCN.

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

Doxychel Hyclate