DOXYCYCLINE HYCLATE tablet, film coated

Country: মার্কিন যুক্তরাষ্ট্র

ভাষা: ইংরেজি

সূত্র: NLM (National Library of Medicine)

সক্রিয় উপাদান:

DOXYCYCLINE HYCLATE (UNII: 19XTS3T51U) (DOXYCYCLINE ANHYDROUS - UNII:334895S862)

থেকে পাওয়া:

Bryant Ranch Prepack

INN (International Name):

DOXYCYCLINE HYCLATE

রচনা:

DOXYCYCLINE ANHYDROUS 100 mg

প্রশাসন রুট:

ORAL

প্রেসক্রিপশন টাইপ:

PRESCRIPTION DRUG

থেরাপিউটিক ইঙ্গিত:

To reduce the development of drug-resistant bacteria and maintain effectiveness of doxycycline hyclate and other antibacterial drugs, doxycycline hyclate should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Treatment: Doxycycline is indicated for the treatment of the following infections: Doxycycline is also indicated for the treatment of infections caused by the following gram-negative microorganisms: Because many strains of the following groups of microorganisms have been shown to be resistant to doxycycline, culture and susceptibility testing are recommended. Doxycycline is indicated for treatment of infections caused by the following gram-negative bacteria, when bacteriologic

পণ্য সারাংশ:

Product: 63629-6880 NDC: 63629-6880-1 30 TABLET, FILM COATED in a BOTTLE NDC: 63629-6880-2 14 TABLET, FILM COATED in a BOTTLE NDC: 63629-6880-3 42 TABLET, FILM COATED in a BOTTLE NDC: 63629-6880-4 28 TABLET, FILM COATED in a BOTTLE NDC: 63629-6880-5 20 TABLET, FILM COATED in a BOTTLE

অনুমোদন অবস্থা:

Abbreviated New Drug Application

পণ্য বৈশিষ্ট্য

DOXYCYCLINE HYCLATE- DOXYCYCLINE HYCLATE TABLET, FILM COATED
BRYANT RANCH PREPACK
----------
DOXYCYCLINE HYCLATE CAPSULES USP 50 MG AND 100 MG DOXYCYCLINE HYCLATE
TABLETS USP 100 MG
RX ONLY
To reduce the development of drug-resistant bacteria and maintain the
effectiveness of doxycycline
hyclate and other antibacterial drugs, doxycycline hyclate should be
used only to treat or prevent
infections that are proven or strongly suspected to be caused by
bacteria.
DESCRIPTION
Doxycycline hyclate is an antibacterial drug synthetically derived
from oxytetracycline, and is available
as doxycycline hyclate (doxycycline hydrochloride hemiethanolate
hemihydrate) capsules and tablets
for oral administration. The chemical designation of this light-yellow
crystalline powder is alpha-6-
deoxy-5-oxytetracycline. Doxycycline has a high degree of lipoid
solubility and a low affinity for
calcium binding. It is highly stable in normal human serum.
Doxycycline will not degrade into an
epianhydro form. Doxycycline hyclate has the following structural
formula:
Each capsule for oral administration contains doxycycline hyclate
equivalent to 50 mg or 100 mg
doxycycline (anhydrous). Inactive ingredients for capsules are:
anhydrous lactose, croscarmellose
sodium, FD&C Blue #1, gelatin, magnesium stearate, microcrystalline
cellulose, and titanium dioxide.
Each tablet for oral administration contains doxycycline hyclate
equivalent to 100 mg doxycycline.
Inactive ingredients for tablets are: anhydrous lactose, carnauba wax,
croscarmellose sodium, D&C
Yellow #10 aluminum lake, FD&C Red #40 aluminum lake, hypromellose,
magnesium stearate,
microcrystalline cellulose, polyethylene glycol, polysorbate 80, and
titanium dioxide.
CLINICAL PHARMACOLOGY
Tetracyclines are readily absorbed and are bound to plasma proteins in
varying degree. They are
concentrated by the liver in the bile and excreted in the urine and
feces at high concentrations and in a
biologically active form. Doxycycline is virtually completely absorbed
after oral administration.
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