Land: USA
Språk: engelsk
Kilde: NLM (National Library of Medicine)
AMPICILLIN SODIUM (UNII: JFN36L5S8K) (AMPICILLIN - UNII:7C782967RD)
Claris Lifesciences, Inc.
AMPICILLIN SODIUM
AMPICILLIN 250 mg
INTRAMUSCULAR
PRESCRIPTION DRUG
Ampicillin for Injection, USP is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the following conditions: Respiratory tract Infections caused by S. pneumoniae (formerly D. pneumoniae ). Staphylococcus aureus (penicillinase and nonpenicillinase-producing), H. influenzae, and Group A beta-hemolytic Streptococci. Bacterial Meningitis caused by E. coli, Group B Streptococci, and other Gram-negative bacteria (Listeria monocytogenes, N. meningitidis ). The addition of an aminoglycoside with ampicillin may increase its effectiveness against Gram-negative bacteria. Septicemia and Endocarditis caused by susceptible Gram-positive organisms including Streptococcus sp., penicillin G-susceptible staphylococci, and enterococci. Gram-negative sepsis caused by E. coli, Proteus mirabilis and Salmonella sp. respond to ampicillin. Endocarditis due to enterococcal strains usually respond to intravenous therapy. The addition of an aminoglycoside may enhance the effe
Ampicillin for Injection, USP for I.M.or I.V. Injection. Each vial contains Ampicillin sodium equivalent to 250, 500 mg, 1 gram or 2 grams ampicillin per vial. Store dry powder at 20° to 25°C (68° to 77°F). [See USP controlled room temperature]. NDC 36000-070-10 250 mg vial packaged in 10s NDC 36000-071-10 500 mg vial packaged in 10s NDC 36000-072-10 1 gram vial packaged in 10s NDC 36000-073-10 2 gram vial packaged in 10s
Abbreviated New Drug Application
AMPICILLIN - AMPICILLIN SODIUM INJECTION, POWDER, FOR SOLUTION CLARIS LIFESCIENCES, INC. ---------- AMPICILLIN FOR INJECTION, USP FOR INTRAMUSCULAR OR INTRAVENOUS INJECTION RX ONLY To reduce the development of drug-resistant bacteria and maintain the effectiveness of Ampicillin for Injection, USP and other antibacterial drugs, Ampicillin for Injection, USP should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION Ampicillin for Injection, USP the monosodium salt of [2S-[2α,5α,6β(S*)]]-6- [(aminophenylacetyl)amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, is a synthetic penicillin. It is an antibacterial agent with a broad spectrum of bactericidal activity against both penicillin-susceptible Gram-positive organisms and many common Gram-negative pathogens. It has the following chemical structure: Ampicillin sodium is a white to off-white crystalline powder with the molecular formula of C H N NaO S, and the molecular weight of 371.39. Each vial of Ampicillin for Injection contains ampicillin sodium equivalent to 250 mg, 500 mg, 1 gram or 2 grams ampicillin. Ampicillin for Injection, USP contains 2.9 milliequivalents of sodium (66 mg of sodium) per 1 gram of drug. CLINICAL PHARMACOLOGY Ampicillin for Injection, USP diffuses readily into most body tissues and fluids. However, penetration into the cerebrospinal fluid and brain occurs only when the meninges are inflamed. Ampicillin is excreted largely unchanged in the urine and its excretion can be delayed by concurrent administration of probenecid. The active form appears in the bile in higher concentrations than those found in serum. Ampicillin is the least serum-bound of all the penicillins, averaging about 20% compared to approximately 60 to 90% for other penicillins. Ampicillin for Injection, USP is well tolerated by most patients and has been given in doses of 2 grams daily for many weeks without adverse reactions. MICROBIOLOGY While _in vitro_ studies have demon read_full_document