BALTINE Duloxetine (as hydrochloride) 60 mg enteric capsules blister pack Australia - inglese - Department of Health (Therapeutic Goods Administration)

baltine duloxetine (as hydrochloride) 60 mg enteric capsules blister pack

dr reddys laboratories australia pty ltd - duloxetine hydrochloride, quantity: 67.3 mg (equivalent: duloxetine, qty 60 mg) - capsule, enteric - excipient ingredients: hypromellose phthalate; triethyl citrate; purified talc; sucrose; hypromellose; glycine; maize starch; titanium dioxide; indigo carmine aluminium lake; purified water; iron oxide yellow; gelatin; acetic acid; silicon dioxide; sodium lauryl sulfate; citric acid; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - indications,1. treatment of major depressive disorder (mdd),2. treatment of diabetic peripheral neuropathic pain (dpnp),3. treatment of generalised anxiety disorder (gad)

DULOXETINE-RZ Duloxetine (as hydrochloride) 60 mg enteric capsules blister pack Australia - inglese - Department of Health (Therapeutic Goods Administration)

duloxetine-rz duloxetine (as hydrochloride) 60 mg enteric capsules blister pack

dr reddys laboratories australia pty ltd - duloxetine hydrochloride, quantity: 67.3 mg (equivalent: duloxetine, qty 60 mg) - capsule, enteric - excipient ingredients: hypromellose phthalate; triethyl citrate; purified talc; sucrose; hypromellose; glycine; maize starch; titanium dioxide; indigo carmine aluminium lake; purified water; iron oxide yellow; gelatin; acetic acid; silicon dioxide; sodium lauryl sulfate; citric acid; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - indications,1. treatment of major depressive disorder (mdd),2. treatment of diabetic peripheral neuropathic pain (dpnp),3. treatment of generalised anxiety disorder (gad)

AMOXICILLIN AND CLAVULANATE POTASSIUM tablet, film coated Stati Uniti - inglese - NLM (National Library of Medicine)

amoxicillin and clavulanate potassium tablet, film coated

preferred pharmaceuticals, inc. - amoxicillin (unii: 804826j2hu) (amoxicillin anhydrous - unii:9em05410q9), clavulanate potassium (unii: q42omw3at8) (clavulanic acid - unii:23521w1s24) - amoxicillin anhydrous 500 mg - to reduce the development of drug‑resistant bacteria and maintain the effectiveness of amoxicillin and clavulanate potassium and other antibacterial drugs, amoxicillin and clavulanate potassium should be used only to treat 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. amoxicillin and clavulanate potassium is a combination penicillin-class antibacterial and beta-lactamase inhibitor indicated in the treatment of infections due to susceptible isolates of the designated bacteria in the conditions listed below*: caused by beta‑lactamase–producing isolates of haemophilus influenzae and moraxella catarrhalis . caused by beta‑lactamase–producing isolates of h. influenzae and m. catarrhalis . caused by beta‑lactamase–pro

amoxicillin and clavulanate potassium- Amoxicillin and clavulanate potassium powder, for suspension
amoxicillin and clavulanate Stati Uniti - inglese - NLM (National Library of Medicine)

amoxicillin and clavulanate potassium- amoxicillin and clavulanate potassium powder, for suspension amoxicillin and clavulanate

ranbaxy pharmaceuticals inc. - amoxicillin (unii: 804826j2hu) (amoxicillin - unii:804826j2hu), clavulanate potassium (unii: q42omw3at8) (clavulanic acid - unii:23521w1s24) - powder, for suspension - 200 mg in 5 ml - amoxicillin and clavulanate potassium for oral suspension, and amoxicillin and clavulanate potassium tablets (chewable) is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the conditions listed below: lower respiratory tract infections - caused by β-lactamase-producing strains of h. influenzae and m. catarrhalis . otitis media - caused by β-lactamase-producing strains of h. influenzae and m. catarrhalis . sinusitis - caused by β-lactamase-producing strains of h. influenzae and m. catarrhalis . skin and skin structure infections - caused by β-lactamase-producing strains of s. aureus , e. coli , and klebsiella spp. urinary tract infections - caused by β-lactamase-producing strains of e. coli , klebsiella spp. and enterobacter spp. while amoxicillin and clavulanate potassium is indicated only for the conditions listed above, infections caused by ampicillin-susceptible organisms are also amenable to treatment with amoxicillin and clavulanate potassium due

AMOXICILLIN AND CLAVULANATE POTASSIUM- amoxicillin and clavulanate potassium tablet, film coated Stati Uniti - inglese - NLM (National Library of Medicine)

amoxicillin and clavulanate potassium- amoxicillin and clavulanate potassium tablet, film coated

nucare pharmaceuticals, inc. - amoxicillin (unii: 804826j2hu) (amoxicillin anhydrous - unii:9em05410q9), clavulanate potassium (unii: q42omw3at8) (clavulanic acid - unii:23521w1s24) - amoxicillin anhydrous 875 mg - to reduce the development of drug‑resistant bacteria and maintain the effectiveness of amoxicillin and clavulanate potassium and other antibacterial drugs, amoxicillin and clavulanate potassium should be used only to treat 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. amoxicillin and clavulanate potassium is a combination penicillin-class antibacterial and beta-lactamase inhibitor indicated in the treatment of infections due to susceptible isolates of the designated bacteria in the conditions listed below*: caused by beta‑lactamase–producing isolates of haemophilus influenzae and moraxella catarrhalis . caused by beta‑lactamase–producing isolates of h. influenzae and m. catarrhalis . caused by beta‑lactamase–pro

P-CARE X- lidocaine hydrochloride, sodium chloride, povidone-iodine, isopropyl alcohol kit Stati Uniti - inglese - NLM (National Library of Medicine)

p-care x- lidocaine hydrochloride, sodium chloride, povidone-iodine, isopropyl alcohol kit

rx pharma-pack, inc. - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - lidocaine hydrochloride anhydrous 10 mg in 1 ml - lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type. sodium chloride injection, usp, 0.9% preparations are indicated for diluting or dissolving drugs for intramuscular, intravenous or subcutaneous injection according to instructions of the manufacturer of the drug to be administered. sodium chloride injection, usp, 0.9% is also indicated for use in flushing of intravenous catheters. antiseptic antiseptic skin preparation antiseptic for preparation of the skin prior to injection.

LIDOCAINE HYDROCHLORIDE injection, solution
LIDOCAINE HYDROCHLORIDE injection, solution Stati Uniti - inglese - NLM (National Library of Medicine)

lidocaine hydrochloride injection, solution lidocaine hydrochloride injection, solution

hikma pharmaceuticals usa inc. - lidocaine hydrochloride (unii: v13007z41a) (lidocaine - unii:98pi200987) - lidocaine hydrochloride anhydrous 10 mg in 1 ml - lidocaine hcl injections are indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed.  lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

AMOXICILLIN AND CLAVULANATE POTASSIUM powder, for suspension Stati Uniti - inglese - NLM (National Library of Medicine)

amoxicillin and clavulanate potassium powder, for suspension

rebel distributors corp - amoxicillin (unii: 804826j2hu) (amoxicillin anhydrous - unii:9em05410q9), clavulanate potassium (unii: q42omw3at8) (clavulanic acid - unii:23521w1s24) - amoxicillin anhydrous 400 mg in 5 ml - amoxicillin and clavulanate potassium is indicated in the treatment of infections caused by susceptible strains of the designated organisms in the conditions listed below: lower respiratory tract infections − caused by β-lactamase−producing strains of h. influenzae and m. catarrhalis . otitis media − caused by β-lactamase−producing strains of h. influenzae and m. catarrhalis . sinusitis − caused by β-lactamase−producing strains of h. influenzae and m. catarrhalis . skin and skin structure infections − caused by β-lactamase−producing strains of s. aureus , e. coli , and klebsiella spp. urinary tract infections − caused by β-lactamase−producing strains of e. coli , klebsiella spp. and enterobacter spp. while amoxicillin and clavulanate potassium is indicated only for the conditions listed above, infections caused by ampicillin-susceptible organisms are also amenable to treatment with amoxicillin and clavulanate potassium due to its amoxicillin content. therefore, mixed infections caused by ampicilli

LIDOCAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE injection, solution Stati Uniti - inglese - NLM (National Library of Medicine)

lidocaine hydrochloride and epinephrine bitartrate injection, solution

iq dental - lidocaine hydrochloride (unii: v13007z41a) (lidocaine - unii:98pi200987), epinephrine bitartrate (unii: 30q7ki53ak) (epinephrine - unii:ykh834o4bh) - lidocaine hydrochloride 20 mg in 1 ml - lidocaine and epinephrine injection, usp is indicated for the production of local anesthesia for dental procedures by nerve block or infiltration techniques. only accepted procedures for these techniques as described in standard textbooks are recommended. lidocaine and epinephrine injections is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type or to any components of the injectable formulations.

LIDOCAINE HYDROCHLORIDE solution Stati Uniti - inglese - NLM (National Library of Medicine)

lidocaine hydrochloride solution

international medication systems, limited - lidocaine hydrochloride (unii: v13007z41a) (lidocaine - unii:98pi200987) - lidocaine hydrochloride anhydrous 40 mg in 1 ml - lidocaine hcl topical solution, 4% is indicated for the production of topical anesthesia of the mucous membranes of the respiratory tract. lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.