United States - English - NLM (National Library of Medicine)

hikma pharmaceuticals usa inc. - phenobarbital sodium (unii: sw9m9bb5k3) (phenobarbital - unii:yqe403bp4d) - phenobarbital sodium 65 mg in 1 ml - - sedative. sedation is obtainable within an hour, and in adequate dosage, the duration of action is more than six hours. included in the more common conditions in which the sedative action of this class of drugs is desired are anxiety-tension states, hyperthyroidism, essential hypertension, nausea and vomiting of functional origin, motion sickness, acute labyrinthitis, pylorospasm in infants, chorea and cardiac failure. phenobarbital is also a useful adjunct in treatment of hemorrhage from the respiratory or gastrointestinal tract. phenobarbital controls anxiety, decreases muscular activity and lessens nervous excitability in hyperthyroid patients. however, thyrotoxic individuals occasionally react poorly to barbiturates. - hypnotic, for the short-term treatment of insomnia, since it appears to lose its effectiveness for sleep induction and sleep maintenance after 2 weeks (see clinical pharmacology ). -  preanesthetic. - long-term anticonvulsant, (phenobarbital, mephobarbital and metharbital) for the treatme

Australia - English - APVMA (Australian Pesticides and Veterinary Medicines Authority)

troy laboratories pty ltd - pentobarbitone sodium - parenteral liquid/solution/suspension - pentobarbitone sodium barbiturate active 60.0 mg/ml - anaesthetics/analgesics - cat | cattle | dog | horse | pigs | sheep | beef | bitch | boar | bos indicus | bos taurus | bovine | buffalo | bull | bullock | - anaesthetic - general

New Zealand - English - Medsafe (Medicines Safety Authority)

sandoz new zealand limited - benzylpenicillin sodium 2994mg equivalent to 5 miu benzylpenicillin sodium salt - powder for injection - 2994 mg - active: benzylpenicillin sodium 2994mg equivalent to 5 miu benzylpenicillin sodium salt

New Zealand - English - Medsafe (Medicines Safety Authority)

sandoz new zealand limited - benzylpenicillin sodium 5988mg equivalent to 10 miu benzylpenicillin sodium salt - powder for injection - 5988 mg - active: benzylpenicillin sodium 5988mg equivalent to 10 miu benzylpenicillin sodium salt

New Zealand - English - Medsafe (Medicines Safety Authority)

sandoz new zealand limited - benzylpenicillin sodium 600mg equivalent to benzylpenicillin 1,000,000 iu (sterile) - powder for injection - 1e+006 iu - active: benzylpenicillin sodium 600mg equivalent to benzylpenicillin 1,000,000 iu (sterile)

Israel - English - Ministry of Health

teva israel ltd - benzylpenicillin sodium - powder for solution for injection - benzylpenicillin sodium 5 miu/vial - benzylpenicillin - benzylpenicillin - infections due to penicillin sensitive organisms.

Israel - English - Ministry of Health

teva israel ltd - benzylpenicillin sodium - powder for solution for injection - benzylpenicillin sodium 10 mu/vial - benzylpenicillin - benzylpenicillin - infections due to penicillin - sensitive microorganisms.

United States - English - NLM (National Library of Medicine)

bryant ranch prepack - warfarin sodium (unii: 6153cwm0cl) (warfarin - unii:5q7zvv76ei) - warfarin sodium tablets, usp are indicated for the prophylaxis and/or treatment of venous thrombosis and its extension, and pulmonary embolism. warfarin sodium tablets, usp are indicated for the prophylaxis and/or treatment of the thromboembolic complications associated with atrial fibrillation and/or cardiac valve replacement. warfarin sodium tablets, usp are indicated to reduce the risk of death, recurrent myocardial infarction, and thromboembolic events such as stroke or systemic embolization after myocardial infarction. anticoagulation is contraindicated in any localized or general physical condition or personal circumstance in which the hazard of hemorrhage might be greater than the potential clinical benefits of anticoagulation, such as: warfarin sodium tablets, usp are contraindicated in women who are or may become pregnant because the drug passes through the placental barrier and may cause fatal hemorrhage to the fetus . furthermore, there have been reports of birth malformations in children born to m

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - levothyroxine sodium, quantity: 50 microgram - tablet, uncoated - excipient ingredients: sodium starch glycollate; sodium stearylfumarate; microcrystalline cellulose; light magnesium oxide - levothox is indicated for the management of demonstrated thyroid hormone deficiency.,levothox is also used to suppress thyrotropin (tsh) for the management of tsh-responsive tumours of the thyroid.

Australia - English - Department of Health (Therapeutic Goods Administration)

accord healthcare pty ltd - levothyroxine sodium, quantity: 200 microgram - tablet, uncoated - excipient ingredients: light magnesium oxide; sodium starch glycollate; sodium stearylfumarate; microcrystalline cellulose; allura red ac aluminium lake - levothox is indicated for the management of demonstrated thyroid hormone deficiency.,levothox is also used to suppress thyrotropin (tsh) for the management of tsh-responsive tumours of the thyroid.