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Norfloxacin (Noroxin)

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Generic Noroxin medication belongs to a class of drugs called quinolone antibiotics. Generic Noroxin is used to treat a variety of bacterial infections. Generic Noroxin works by stopping the growth of bacteria.

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Alenbit, Ambigram, Amicrobin, Apiflox, Apirol, Asudufe, Azo uroflam, Baccidal, Bacfamil, Bacteriotal, Bactracid, Bafurokisaru, Barazan, Barocul, Basteen, Baxicin, Bexinor, Bio tarbun, Biscolet, Blemalart, Chibroxin, Chibroxine, Chibroxol, Co norfloxacin, Constilax, Danilon, Diperflox, Effectsal, Epinor, Esclebin, Espeden, Firin, Flobarl, Flocidal, Flossac, Flox, Floxamed, Floxamicin, Floxatral, Floxatrat, Floxen, Floxinol, Fluseminal, Foxgoria, Grenis, Gyrablock, H-norfloxacin, Janacin, Lemorcan, Lexiflox, Lexinor, Lorcamin, Loxone, Mariotton, Memento nf, Menorox, Microxin, Mitatonin, N-flox, Naflox, Nalion, Negaflox, Negalflex, Niterat, Noflo, Nofloxan, Nofocin, Nofxan, Nolicin, Noprose, Nor, Noracin, Norax, Noraxin, Norbactin, Norcozine, Norfacin, Norfen, Norflodal, Norflogen, Norflohexal, Norflok, Norflol, Norflomax, Norflosal, Norilet, Normax, Norocin, Noroxine, Norsol, Norzen, Notler, Noxacin, Nufloxib, Oranor, Ovinol, Parcetin, Pharex norfloxacin, Pistofil, Quinabic, Renor, Renoxacin, Respexil, Rexacin, Ritromine, Sebercim, Senro, Setanol, Shinun, Sinobid, Sofasin, Stbanil, Taflox, Theanorf, Trizolin, Unasera, Uricin, Uriflox, Uritracin, Uroflox, Urofos, Uronovag, Uroquin, Uroseptal, Urospes-n, Urotem, Uroxacin, Utibid, Uticina, Utinor, Vefloxa, Vetamol, Wenflox, Xaflor, Xasmun, Zoroxin

Similar Products:
Cipro, Levaquin, Quixin, Tequin, Avelox, Ocuflox


Also known as:  Noroxin.


Generic Noroxin medication belongs to a class of drugs called quinolone antibiotics. Generic Noroxin works by stopping the growth of bacteria.

Generic Noroxin should not be used for colds, flu, other virus infections, sore throats or other minor infections, or to prevent infections.

Noroxin is also known as Norfloxacin, Norfloxacine, Apo-Norflox, Norflohexal, Roxin, Utinor.

Generic name of Generic Noroxin is Norfloxacin.

Brand name of Generic Noroxin is Noroxin.


Take Generic Noroxin orally with a full glass of water.

Take Generic Noroxin usually twice a day, at least 1 hour before or at least 2 hours after a meal or dairy products (e.g., milk, yogurt).

Take Generic Noroxin 2 hours before or 2 hours after taking any products containing magnesium, aluminum or calcium.

The dosage of tablets depends on the disease and its prescribed treatment.

If you want to achieve most effective results do not stop taking Generic Noroxin suddenly.


If you overdose Generic Noroxin and you don't feel good you should visit your doctor or health care provider immediately.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Keep bottle closed tightly. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Norfloxacin are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Do not take Generic Noroxin if you are allergic to Generic Noroxin components or to quinolone antibiotics such as ciprofloxacin, gatifloxacin, gemifloxacin, levofloxacin, lomefloxacin, moxifloxacin or ofloxacin.

Generic Noroxin should not be used for colds, flu, other virus infections, sore throats or other minor infections, or to prevent infections.

Be careful if you are pregnant, planning to become pregnant, or are breast-feeding.

Be careful if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement.

Be careful if you have seizures, brain disorders (e.g., cerebral arteriosclerosis, tumor, increased intracranial pressure), muscle disease/weakness (e.g., myasthenia gravis), heart problems (e.g., cardiomyopathy, slow heart rate, torsades de pointes, QTc interval prolongation), kidney disease, mineral imbalance (e.g., low potassium or magnesium), history of tendonitis/tendon problems.

When you take Generic Noroxin you should drink plenty of fluids.

Avoid alcohol and beverages containing caffeine (coffee, tea, colas), do not eat large amounts of chocolate.

Avoid prolonged sun exposure, tanning booths or sunlamps. Use a sunscreen and wear protective clothing when outdoors.

It can be dangerous to stop Generic Noroxin taking suddenly.

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The drug resistance of clinical isolates of S. paratyphi A was serious in Dengfeng, Henan province, PFGE patterns showed a diversity, but predominant patterns could also be found. The PFGE patterns of some strains had clustering and were related with their antidrug spectrums.

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(1) S. epidermidis, S. haemolyticus, and S. saprophyticus accounted for 82.2% of the CoNS isolated from Chengdu, with different constituent ratio of CoNS among patients, medical staff, sick children and normal people. (2) CoNS resisted to one or more antimicrobial agents with resistance rate of 80.4% . CoNS resisted highly to SMZ, penicillin-G, ampicillin, erythromycin, TMP-SMZ and tetracycline, but were susceptible to vancomycin, norfloxacin and amikacin. 25 antimicrobial resistance profiles were acquired, and Amp + Ery + P-G + SMZ, Amp + Gen + Str + Tet, Amp + P-G + Tet, Chl + Ery + P-G + SMZ + TS, Ern + Nov + P-G + SMZ + TS, as well as P-G + SMZ + TS were main profiles. The main antimicrobial resistance profiles of CoNS isolated from patients, medical staff, sick children and normal people had some differences, but the antimicrobial resistance of main biochemical subtypes was similar a lot. (3) Plasmid prevalence of CoNS was 72.9%, with 12 plasmid profiles ( I -H ) of all CoNS. The main profiles were I , U , and MI type, which accounted for 80.1% of 1485 CoNS with plasmid. (4) 29 PFGE genotypes and 112 subtypes were found in 2038 strains. Genotypes A, B, C, D and E were the predominant types in CoNS from patients, medical staff, sick children and normal people and contributed 89.1% to 2038 CONS. Genotypes A was the major type and had similar constituent ratio in CoNS from 4 sources, and no enough similarity of constituent ratio in other dominant genotypes.

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This is the first report on drug resistance-modifying potential of CD through inhibition of MDR efflux pump.

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The mean age was 52.2 years. All patients had the characteristic disseminated, punctate, slightly elevated, white epithelial lesions. The denser white lesions could be removed easily after gentle swabbing, and most epithelium remained intact. The 10 cases with positive polymerase chain reaction results were all identified to be Vittaforma corneae. The mean number of corneal swabbing was 3.3, and the mean disease resolution time was 6.6 days. No patients had recurrence or loss of visual acuity at last follow-up.

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Urinary Tract Infections (UTIs) are the most common serious bacterial infections which are seen during infancy. The aim of the present study was to evaluate aetiology, and antimicrobial resistance patterns among infants and children who approached our hospital for treatment of UTIs.

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This Article reports a detailed characterization of the binding interaction of a potential chemotherapeutic antibacterial drug, norfloxacin (NOF), with the mammalian milk protein β-lactoglobulin (βLG). The thermodynamic parameters, ΔH, ΔS, and ΔG, for the binding phenomenon as-evaluated on the basis of van't Hoff relationship reveal the predominance of electrostatic/ionic interactions underlying the binding process. However, the drug-induced quenching of the intrinsic tryptophanyl fluorescence of the protein exhibits intriguing characteristics on Stern-Volmer analysis (displays an upward curvature instead of conforming to a linear regression). Thus, an extensive time-resolved fluorescence spectroscopic characterization of the quenching process has been undertaken in conjugation with temperature-dependent fluorescence quenching studies to unveil the actual quenching mechanism. The invariance of the fluorescence decay behavior of βLG as a function of the quencher (here NOF) concentration coupled with the commensurate dependence of the drug-protein binding constant (K) on temperature, the drug-induced fluorescence quenching of βLG is argued to proceed through static mechanism. This postulate is aided further support from absorption, fluorescence, and circular dichroism (CD) spectral studies. The present study also throws light on the important issue of drug-induced modification in the native protein conformation on the lexicon of CD, excitation-emission matrix spectroscopic techniques. Concurrently, the drug-protein interaction kinetics and the energy of activation of the process are also explored from stopped-flow fluorescence technique. The probable binding locus of NOF in βLG is investigated from AutoDock-based blind docking simulation.

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buy norfloxacin 2015-02-02

The efficacy and safety of rufloxacin (400 mg, single dose) were compared to those of norfloxacin (400 mg twice a day for 3 days) for the treatment of women with uncomplicated cystitis. In addition, urine levels, drug level/MIC ratio, and urine antibacterial activity 72 to 84 h after treatment initiation were determined in a subgroup of patients for pharmacodynamic assessment. A total of 203 women were included and treated in this open, randomized clinical trial; 100 patients received norfloxacin, whereas 103 received rufloxacin. Of these, 156 (74 and 82 patients in the norfloxacin and rufloxacin groups, respectively) were considered bacteriologically evaluable. At the first follow-up visits (3 to 12 days after starting the treatment), bacteriological cure rates were 99 and 94% for norfloxacin and rufloxacin, respectively. Seventy-nine percent (119 of 150) of bacteriologically cured patients attended a long-term follow-up visit (4 to 6 weeks after starting the treatment), where a relapse rate of 4% (2 of 54) and 5% (3 of 64) were found in the norfloxacin and rufloxacin groups, respectively. The pharmacodynamic evaluation performed in 35 patients showed similar median urine levels (approximately equal to 25 micrograms/ml) and urine antibacterial activity for both treatment groups against initial isolates, despite a higher norfloxacin level/MIC ratio due to the lower MIC of norfloxacin. Twenty- buy norfloxacin one patients (20%) in the rufloxacin group and 12 patients (12%) in the norfloxacin group reported 39 and 16 adverse events, respectively, almost all of them being mild and lasting < 24 h. Overall, gastrointestinal reactions were the most frequent adverse events reported. However, 12 patients treated with rufloxacin reported 15 central nervous system adverse events. This study shows that single doses of rufloxacin are as effective as a norfloxacin 3-day standard treatment in uncomplicated cystitis. The results obtained with rufloxacin are consistent with its pharmacodynamic properties.

where to buy norfloxacin 2017-09-02

The Drug-Resistant Pathogen Surveillance Group in Pediatric Infectious Disease has conducted surveillance of pediatric patients with respiratory tract infections, meningitis, and sepsis five times (in 2000-2001 [period 1], 2004 [period 2], 2007 [period 3], 2010 [period 4], and 2012 [period 5]). With respect to the clinically isolated Haemophilus influenzae, the drug susceptibility, the frequency of drug-resistant strains, and patients' background factors in each period have already been reported. Here we evaluate trends in the development of drug resistance in H. influenzae, and the relationship between the development of drug resistance and patients' background factors in the aforementioned five periods. H. influenzae derived from pediatric patients with respiratory tract infections that had been previously collected (period 1, 448 isolates; period 2, 376 isolates; period 3, 386 isolates; period 4, 484 isolates; and period 5, 411 isolates) were analyzed. The proportions of ß-lactamase-nonproducing ampicillin (ABPC)-intermediate resistant (BLNAI) strains + β-lactamase-nonproducing ABPC-resistant (BLNAR) strains were 28.8% in period 1, 59.3% in period 2, 61.1% in period 3, 58.1% in period 4, and 63.5% in period 5, showing a rapid increase from period 1 to period 2 followed by an almost constant rate of approximately Buy Azithromycin Tablets Online 60%. The proportion of ß-lactamase-producing ABPC-resistant (BLPAR) strains + ß-lactamase-producing clavulanic acid/amoxicillin-resistant (BLPACR) strains was 4.4% in period 3, which was somewhat low; however, there were no significant changes in the proportions of these strains, which ranged between 6.4% and 8.7% throughout the surveillance period except for period 3. The drugs whose MIC90 values against BLNAR strains were low throughout the surveillance included piperacillin (0.25 μg/mL) and tazobactam/piperacillin (0.125-0.25 μg/mL) in the penicillins; cefditoren and ceftriaxone (0.25-0.5 μg/mL for both) in the cephems; meropenem (0.5-1 μg/mL) and tebipenem (1 μg/mL) in the carbapenems; and levofloxacin, tosufloxacin, and garenoxacin (≤ 0.06 μg/mL for all) and norfloxacin (0.06-0.125 μg/mL) in the quinolones. We investigated the relationship between the frequency of BLNAS strains/BLNAI + BLNAR strains and patients' background factors in each surveillance period. Significant differences were shown on age category (< 3 years or ≥ 3 years) in all periods except period 4, and the presence/absence of prior administration of antimicrobial agents within one month in period 2 and period 3. In all periods, the frequency of BLNAI + BLNAR strains were higher in patients aged < 3 years than in patients aged ≥ 3 years, and were also higher in patients with presence of prior treatment than in patients without prior treatment. We consider that it is important to promote the proper use of antimicrobial agents by conducting surveillance continuously in the future to clarify the relationship between the development of drug resistance in H. influenzae and patients' background factors and provide those information to clinical setting.

buy norfloxacin 400mg 2016-07-01

Although a clinically relevant interaction between a fluoroquinolone and a metal cation was first described more than 20 years ago the biopharmaceutical mechanism of this interaction is still not understood. One of the obvious disagreements in the literature is about the effect of metal cations on the solubility of fluoroquinolones. Namely, metal cations are Buy Generic Cephalexin reported to increase the solubility of fluoroquinolones as well as to decrease it and thus cause the lowered bioavailability. Thus in this work the solubility of ciprofloxacin, norfloxacin and ofloxacin and the effect of metal cations on the solubility of these fluoroquinolones in aqueous media of different pH values were reevaluated. The results clearly show that the metal cations either do not affect or even increase the solubility of fluoroquinolones. Thus they surely do not influence the bioavailability of these drugs by decreasing their solubility. Additionally, possible explanations for the contradictory results reported in the literature are given.

buy norfloxacin uk 2015-07-27

Bacterial adherence of E. coli obtained Buy Tetracycline For Dogs from patients with cirrhosis is unrelated to the sensitivity/resistance to quinolones, and is similarly reduced in both cases when subminimum inhibitory concentration of norfloxacin is added to the medium.

buy norfloxacin online 2017-04-09

A narrative literature review was performed. In addition the individual patient data (IPD) of 466 females with uncomplicated UTI of four prospective, single blind, randomized, clinical studies with similar protocols using nitroxoline (250 mg tid) versus cotrimoxazole (960 mg bid) or norfloxacin (400 mg bid) as controls for 5 days (sporadic UTI) or 10 days (recurrent UTI) were meta-analysed. The primary aim was eradication of bacteriuria 7-13 days after end of therapy (test of cure). Clinical Buy Azithromycin Antibiotic Online efficacy was determined by elimination of symptoms and safety by adverse events and laboratory tests.

buy norfloxacin online australia 2015-02-18

The combination disk synergy test was used to evaluate 202 consecutive non-repeated Klebsiella pneumoniae (K. pneumonia) strains for ESBL production. The strains were isolated from various Buy Amoxicillin Online Uk clinical specimens of hospitalized patients over the period from July 2005 to March 2007. Their antibiotic susceptibility pattern was also determined by the disk diffusion method. Demographic and medical data of the patients were recorded using a questionnaire.