DOXY

This brand name is authorized in United States. It is also authorized in France, Hong Kong SAR China, Israel, New Zealand, Nigeria.

Active ingredients

The drug DOXY contains one active pharmaceutical ingredient (API):

1
UNII 19XTS3T51U - DOXYCYCLINE HYCLATE
 

Doxycycline is primarily bacteriostatic and is believed to exert its antimicrobial effect by the inhibition of protein synthesis.

 
Read more about Doxycycline

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 DOXY Powder for solution for injection MPI, US: SPL/Old FDA, National Drug Code (US)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
J01AA02 Doxycycline J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01A Tetracyclines → J01AA Tetracyclines
Discover more medicines within J01AA02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
FR Base de données publique des médicaments 61722191, 67061569
HK Department of Health Drug Office 38107, 42036
IL מִשְׂרַד הַבְּרִיאוּת 3532
NG Registered Drug Product Database B4-7010
Switch country to Nigeria in order to find specific presentations of DOXY
NZ Medicines and Medical Devices Safety Authority 2731, 2733
US FDA, National Drug Code 51662-1402, 52584-028, 63323-130

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