Negara: Amerika Serikat
Bahasa: Inggris
Sumber: NLM (National Library of Medicine)
DOXYCYCLINE (UNII: N12000U13O) (DOXYCYCLINE ANHYDROUS - UNII:334895S862)
Sun Pharmaceutical Industries, Inc.
DOXYCYCLINE
DOXYCYCLINE ANHYDROUS 50 mg
ORAL
PRESCRIPTION DRUG
To reduce the development of drug-resistant bacteria and maintain effectiveness of doxycycline capsules, USP and other antibacterial drugs, doxycycline capsules, USP 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. Doxycycline capsules, USP are indicated for the treatment of the following infections: Rocky Mountain spotted fever, typhus fever and the typhus group, Q fever, rickettsialpox, and tick fevers caused by Rickettsiae. Respiratory tract infections caused by Mycoplasma pneumoniae . Lymphogranuloma venereum caused by Chlamydia trachomatis . Psittacosis (ornithosis) caused by Chlamydophila psittaci . Trachoma caused by Chlamydia trachomatis , although the infectious agen
Doxycycline capsules, USP 50 mg have light greenish yellow powder filled in size ‘4’ blue opaque cap/blue opaque body, hard gelatin capsules, imprinted with “RX614” on cap and body in black ink. Each capsule contains doxycycline monohydrate, USP equivalent to 50 mg of doxycycline. Doxycycline capsules, USP 50 mg are available in: Bottles of 20 capsules NDC 63304-614-20 Bottles of 100 capsules NDC 63304-614-01 Bottles of 120 capsules NDC 63304-614-13 Bottles of 500 capsules NDC 63304-614-05 Doxycycline capsules, USP 75 mg have light greenish yellow powder filled in size ‘3’ reflex blue opaque cap/blue opaque body, hard gelatin capsules, imprinted with “RX615” on cap and body in black ink. Each capsule contains doxycycline monohydrate, USP equivalent to 75 mg of doxycycline. Doxycycline capsules, USP 75 mg are available in: Bottles of 100 capsules NDC 63304-615-01 Bottles of 500 capsules NDC 63304-615-05 Unit-dose blister pack of 1 capsule NDC 63304-615-11 Doxycycline capsules, USP 100 mg have light greenish yellow powder filled in size ‘2’ reflex blue opaque cap/blue opaque body, hard gelatin capsules, imprinted with “RX616” on cap and body in black ink. Each capsule contains doxycycline monohydrate, USP equivalent to 100 mg of doxycycline. Doxycycline capsules, USP 100 mg are available in: Bottles of 20 capsules NDC 63304-616-20 Bottles of 100 capsules NDC 63304-616-01 Bottles of 120 capsules NDC 63304-616-13 Bottles of 500 capsules NDC 63304-616-05 Dispense in a tight, light-resistant container as defined in the USP/NF. Store at 20° - 25° C (68° - 77° F) [See USP Controlled Room Temperature]. Protect from light. To report SUSPECTED ADVERSE REACTIONS, contact the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .
Abbreviated New Drug Application
DOXYCYCLINE- DOXYCYCLINE CAPSULE SUN PHARMACEUTICAL INDUSTRIES, INC. ---------- PACKAGE/LABEL DISPLAY PANEL DOXYCYCLINE CAPSULES, USP RX ONLY To reduce the development of drug-resistant bacteria and maintain the effectiveness of doxycycline capsules, USP and other antibacterial drugs, doxycycline capsules, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Doxycycline is a broad-spectrum antibacterial synthetically derived from oxytetracycline. Doxycycline capsules, USP 100 mg, 75 mg, and 50 mg contain doxycycline monohydrate, USP equivalent to 100 mg, 75 mg, or 50 mg of doxycycline for oral administration. The chemical designation of the yellow crystalline powder is 4-(Dimethylamino)-1,4,4a,5,5a,6, 11,12a-octahydro-3,5,10,-12,12a-pentahydroxy- 6-methyl-1,11-dioxo-2-naphthacene-carboxamide monohydrate. Structural formula: Doxycycline has a high degree of lipid solubility and a low affinity for calcium binding. It is highly stable in normal human serum. Doxycycline will not degrade into an epianhydro form. Each capsule for oral administration contains doxycycline monohydrate, USP equivalent to 50 mg, 75 mg or 100 mg of doxycycline. In addition, each capsule contains the following inactive ingredients: colloidal silicon dioxide, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate. The capsule shell contains D&C Red No. 28, FD&C Blue No. 1, gelatin, and titanium dioxide. The edible printing ink contains black iron oxide, potassium hydroxide, propylene glycol, and shellac. CLINICAL PHARMACOLOGY Tetracyclines are readily absorbed and are bound to plasma proteins in varying degrees. They are concentrated by the liver in the bile and excreted in the urine and feces at high concentrations in a biologically active form. Doxycycline is virtually completely absorbed after oral administration. Following a 200 mg dose of doxycycline monohydrate, 24 normal adult volunteers averaged the following serum concentration values: T Baca dokumen lengkapnya