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Drug Catalog - Product Detail

CEFPODOXIME PROXETIL TAB 200 MG 20 CT

NDC Mfr Size Str Form
42043-0121-20 ORCHIDPHARMA 20 200MG TABLET
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Description
DESCRIPTION Cefpodoxime proxetil USP is an orally administered, extended spectrum, semi-synthetic antibiotic of the cephalosporin class. The chemical name is (RS)-1(isopropoxycarbonyloxy) ethyl(+)-(6R,7R)-7-[2-(2-amino-4-thiazolyl)-2-{(Z)methoxyimino}acetamido]-3-methoxymethyl-8-oxo-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxylate. Its empirical formula is C 21 H 27 N 5 O 9 S 2 and its structural formula is represented below: The molecular weight of cefpodoxime proxetil USP is 557.6. Cefpodoxime proxetil USP is a prodrug; its active metabolite is cefpodoxime. All doses of cefpodoxime proxetil USP in this insert are expressed in terms of the active cefpodoxime moiety. The drug is supplied as film-coated tablets. Cefpodoxime proxetil tablets USP 100 mg contain FD&C Yellow No. 5 (tartrazine) and FD&C Yellow No. 6 as color additives. Cefpodoxime proxetil tablets USP 200 mg contain color additives including FD&C Yellow No. 6. Cefpodoxime proxetil tablets USP contain cefpodoxime proxetil USP equivalent to 100 mg or 200 mg of cefpodoxime activity and the following inactive ingredients: carboxymethylcellulose calcium, croscarmellose sodium, sodium lauryl sulfate, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate and opadry orange. The constituents of opadry orange 03H53614 (used in 100 mg strength) are hypromellose, titanium dioxide, propylene glycol, FD&C Yellow No. 5 (tartrazine) and FD&C Yellow No. 6. The constituents of opadry orange 03H53615 (used in 200 mg strength) are hypromellose, titanium dioxide, propylene glycol, FD&C Yellow No. 6 and FD&C Red No. 40. chemstruct
How Supplied
HOW SUPPLIED Cefpodoxime proxetil tablets USP are available in the following strengths (cefpodoxime equivalent), colors, and size: 100 mg, (orange, elliptical, film-coated, with “522” on one side and plain on the other side) Bottles of 20 NDC 42043-120-20 Bottles of 100 NDC 42043-120-01 200 mg, (wine red, elliptical, film-coated, with “523” on one side and plain on the other side) Bottles of 20 NDC 42043-121-20 Bottles of 100 NDC 42043-121-01 Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Replace cap securely after each opening.
Indications & Usage
INDICATIONS AND USAGE Cefpodoxime proxetil tablets are indicated for the treatment of patients with mild to moderate infections caused by susceptible strains of the designated microorganisms in the conditions listed below. Recommended dosages, durations of therapy, and applicable patient populations vary among these infections. Please see DOSAGE AND ADMINISTRATION for specific recommendations. Acute otitis media caused by Streptococcus pneumoniae (excluding penicillin-resistant strains), Streptococcus pyogenes, Haemophilus influenzae (including beta- lactamase-producing strains), or Moraxella (Branhamella) catarrhalis (including beta- lactamase-producing strains). Pharyngitis and/or tonsillitis caused by Streptococcus pyogenes . NOTE: Only penicillin by the intramuscular route of administration has been shown to be effective in the prophylaxis of rheumatic fever. Cefpodoxime proxetil tablets are generally effective in the eradication of streptococci from the oropharynx. However, data establishing the efficacy of cefpodoxime proxetil tablets for the prophylaxis of subsequent rheumatic fever are not available. Community-acquired pneumonia caused by S. pneumoniae or H. influenzae (including beta-lactamase-producing strains). Acute bacterial exacerbation of chronic bronchitis caused by S. pneumoniae , H. influenzae (non-beta-lactamase-producing strains only), or M. catarrhalis . Data are insufficient at this time to establish efficacy in patients with acute bacterial exacerbations of chronic bronchitis caused by beta-lactamase-producing strains of H. influenzae . Acute, uncomplicated urethral and cervical gonorrhea caused by Neisseria gonorrhoeae (including penicillinase-producing strains). Acute, uncomplicated ano-rectal infections in women due to Neisseria gonorrhoeae (including penicillinase-producing strains). NOTE: The efficacy of cefpodoxime in treating male patients with rectal infections caused by N. gonorrhoeae has not been established. Data do not support the use of cefpodoxime proxetil tablets in the treatment of pharyngeal infections due to N. gonorrhoeae in men or women. Uncomplicated skin and skin structure infections caused by Staphylococcus aureus (including penicillinase-producing strains) or Streptococcus pyogenes . Abscesses should be surgically drained as clinically indicated. NOTE: In clinical trials, successful treatment of uncomplicated skin and skin structure infections was dose-related. The effective therapeutic dose for skin infections was higher than those used in other recommended indications. (See DOSAGE AND ADMINISTRATION .) Acute maxillary sinusitis caused by Haemophilus influenzae (including beta-lactamase- producing strains), Streptococcus pneumoniae , and Moraxella catarrhalis . Uncomplicated urinary tract infections (cystitis) caused by Escherichia coli , Klebsiella pneumoniae , Proteus mirabilis , or Staphylococcus saprophyticus . NOTE: In considering the use of cefpodoxime proxetil tablets in the treatment of cystitis, cefpodoxime proxetil's lower bacterial eradication rates should be weighed against the increased eradication rates and different safety profiles of some other classes of approved agents. (See CLINICAL STUDIES section.) Appropriate specimens for bacteriological examination should be obtained in order to isolate and identify causative organisms and to determine their susceptibility to cefpodoxime. Therapy may be instituted while awaiting the results of these studies. Once these results become available, antimicrobial therapy should be adjusted accordingly. To reduce the development of drug-resistant bacteria and maintain the effectiveness of cefpodoxime proxetil tablets and other antibacterial drugs, cefpodoxime proxetil tablets 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.
Dosage and Administration
DOSAGE AND ADMINISTRATION (See INDICATIONS AND USAGE for indicated pathogens.)