B-30 SOLUTION Canada - English - Health Canada

b-30 solution

gea farm technologies inc - polyoxyethylene glycol iodine complex; nonyl phenoxypolyethoxyethanol-iodine complex; alkyl phenol polyglycol ether iodine complex; glycerine - solution - 5.31%; 2.584%; 2.584%; 10.00% - polyoxyethylene glycol iodine complex 5.31%; nonyl phenoxypolyethoxyethanol-iodine complex 2.584%; alkyl phenol polyglycol ether iodine complex 2.584%; glycerine 10.00% - cattle

Intralipid New Zealand - English - Medsafe (Medicines Safety Authority)

intralipid

fresenius kabi new zealand limited - soya oil 30%{relative};  ;   - solution for infusion - 30 % - active: soya oil 30%{relative}     excipient: egg lecithin glycerol water for injection - part of the intravenous diet in all parenteral nutrition indications including: - preoperative and postoperative nutritional disturbances where an improved nitrogen balance is required; - nutritional disorders or disturbances of nitrogen balance due to inadequate or failing intestinal absorption caused by tumours in the gastrointestinal tract, acute or chronic intestinal diseases (peritonitis, ulcerative colitis, terminal ileitis); - burns, to reduce the frequently excessive nitrogen losses; - prolonged unconsciousness, eg following cranial trauma or poisoning in cases where enteral feeding is inappropriate or impossible; - impaired renal function where a concentrated source of energy may be indicated to reduce protein breakdown; - cachexia and - patients with essential fatty acid deficiency who cannot maintain or restore a normal essential fatty acid pattern by oral intake.

HANDY QUAT- benzalkonium chloride soap United States - English - NLM (National Library of Medicine)

handy quat- benzalkonium chloride soap

abc compounding co., inc. - n-alkyl ethylbenzyl dimethyl ammonium chloride (c12-c14) (unii: g258tfn61x) (n-alkyl ethylbenzyl dimethyl ammonium (c12-c14) cation - unii:85440928rv), benzalkonium chloride (unii: f5um2km3w7) (benzalkonium - unii:7n6jud5x6y) - n-alkyl ethylbenzyl dimethyl ammonium chloride (c12-c14) 12.5 mg in 1 ml - antiseptic for hand-washing to decrease bacteria on the skin irritation and redness develop

ROPIVACAINE ACTAVIS 0.5% (w/v) ropivacaine hydrochloride (as monohydrate) 50mg/10mL solution for injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

ropivacaine actavis 0.5% (w/v) ropivacaine hydrochloride (as monohydrate) 50mg/10ml solution for injection ampoule

medis pharma pty ltd - ropivacaine hydrochloride monohydrate, quantity: 52.9 mg - injection, solution - excipient ingredients: sodium chloride; hydrochloric acid; water for injections; sodium hydroxide - surgical anaesthesia (adults and children over 12 years of age),? epidural block for surgery including caesarean section,? intrathecal anaesthesia,? field block (minor nerve block and infiltration),? major nerve block,analgesia (adults and children over 12 years of age),? continuous epidural infusion or intermittent bolus epidural administration for analgesia in postoperative pain or labour pain,? field block (minor nerve block and infiltration),? continuous peripheral nerve block infusion or intermittent injections for post operative pain management,? continuous wound infusion for postoperative pain management (adults only),analgesia (children aged 0 - 12 years),? caudal epidural block in neonates (> 37 weeks gestation and over 2500 g weight), infants and children up to and including 12 years,? continuous epidural infusion in infants (> 30 days and over 2500 g weight) and children up to and including 12 years,? peripheral nerve block in children aged 1 up to and including 12 years,for peri- and postoperative pain management.,there are no safety or efficacy data to support the use of ropivacaine actavis for analgesia for longer than 72 hours. (data for peripheral nerve block administered as a continuous peripheral infusion or intermittent injections and for continuous wound infusion support the use for up to 48 hours only).

Tambocor 10 mg/ml Solution for Injection or Infusion Ireland - English - HPRA (Health Products Regulatory Authority)

tambocor 10 mg/ml solution for injection or infusion

mylan ire healthcare limited - flecainide acetate - solution for injection/infusion - 10 milligram(s)/millilitre - antiarrhythmics, class ic; flecainide

Fluorouracil 50 mg/ml solution for injection or infusion Ireland - English - HPRA (Health Products Regulatory Authority)

fluorouracil 50 mg/ml solution for injection or infusion

accord healthcare ireland ltd. - fluorouracil - solution for injection/infusion - 50 milligram(s)/millilitre - pyrimidine analogues; fluorouracil

Haldol Decanoate 50mg/ml Solution for Injection Ireland - English - HPRA (Health Products Regulatory Authority)

haldol decanoate 50mg/ml solution for injection

janssen sciences ireland uc - haloperidol - solution for injection - 50 milligram(s)/millilitre - butyrophenone derivatives; haloperidol

KETAMINE INTERPHARMA ketamine (as hydrochloride) 500 mg/10 mL solution for injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

ketamine interpharma ketamine (as hydrochloride) 500 mg/10 ml solution for injection ampoule

interpharma pty ltd - ketamine hydrochloride, quantity: 57.67 mg/ml (equivalent: ketamine, qty 50 mg/ml) - injection, solution - excipient ingredients: water for injections; sodium hydroxide; hydrochloric acid - ketamine interpharma? is recommended:,1. as the sole anaesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. ketamine interpharma ? is best suited for short procedures and it can be used with additional doses, for longer procedures; 2. for the induction of anaesthesia prior to the administration of other general anaesthetic agents; 3. to supplement low-potency agents, such as nitrous oxide.

KETAMINE INTERPHARMA ketamine (as hydrochloride) 100 mg/2 mL solution for injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

ketamine interpharma ketamine (as hydrochloride) 100 mg/2 ml solution for injection ampoule

interpharma pty ltd - ketamine hydrochloride, quantity: 57.67 mg/ml (equivalent: ketamine, qty 50 mg/ml) - injection, solution - excipient ingredients: hydrochloric acid; water for injections; sodium hydroxide - ketamine interpharma? is recommended:,1. as the sole anaesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. ketamine interpharma ? is best suited for short procedures and it can be used with additional doses, for longer procedures; 2. for the induction of anaesthesia prior to the administration of other general anaesthetic agents; 3. to supplement low-potency agents, such as nitrous oxide.

KETAMINE INTERPHARMA ketamine (as hydrochloride) 250 mg/5 mL solution for injection ampoule Australia - English - Department of Health (Therapeutic Goods Administration)

ketamine interpharma ketamine (as hydrochloride) 250 mg/5 ml solution for injection ampoule

interpharma pty ltd - ketamine hydrochloride, quantity: 57.67 mg/ml (equivalent: ketamine, qty 50 mg/ml) - injection, solution - excipient ingredients: sodium hydroxide; water for injections; hydrochloric acid - ketamine interpharma? is recommended:,1. as the sole anaesthetic agent for diagnostic and surgical procedures that do not require skeletal muscle relaxation. ketamine interpharma ? is best suited for short procedures and it can be used with additional doses, for longer procedures; 2. for the induction of anaesthesia prior to the administration of other general anaesthetic agents; 3. to supplement low-potency agents, such as nitrous oxide.