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

lannett company, inc. - levorphanol tartrate (unii: 04wqu6t9qi) (levorphanol - unii:27618j1n2x) - levorphanol tartrate tablets are indicated for the management of pain severe enough to require an opioid analgesic and for which alternative treatments are inadequate. limitations of use because of the risks of addiction, abuse, and misuse, with opioids, even at recommended doses [see warnings ], reserve levorphanol tartrate tablets for use in patients for whom alternative treatment options [e.g., non-opioid analgesics or opioid combination products]: - have not been tolerated, or are not expected to be tolerated, - have not provided adequate analgesia, or are not expected to provide adequate analgesia levorphanol tartrate tablets are contraindicated in patients with: - significant respiratory depression [see warnings ] - acute or severe bronchial asthma in an unmonitored setting or in the absence of resuscitative equipment [see warnings ] - known or suspected gastrointestinal obstruction, including paralytic ileus [see warnings ]  - hypersensitivity to levorphanol or any of the formulation excipients

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

lannett company, inc. - doxepin hydrochloride (unii: 3u9a0fe9n5) (doxepin - unii:5asj6huz7d) - doxepin hydrochloride is recommended for the treatment of:     1. psychoneurotic patients with depression and/or anxiety.     2. depression and/or anxiety associated with alcoholism (not to be taken concomitantly with alcohol).     3. depression and/or anxiety associated with organic disease (the possibility of drug interaction should be considered if the patient is receiving other drugs concomitantly).     4. psychotic depressive disorders with associated anxiety including involutional depression and manic-depressive disorders. the target symptoms of psychoneurosis that respond particularly well to doxepin hydrochloride include anxiety, tension, depression, somatic symptoms and concerns, sleep disturbances, guilt, lack of energy, fear, apprehension and worry. clinical experience has shown that doxepin hydrochloride is safe and well tolerated even in the elderly patient. owing to lack of clinical experience in the pediatric population, doxepin hydrochloride is not recommended for use in children under 12 year

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

lannett company, inc. - methylphenidate hydrochloride (unii: 4b3sc438hi) (methylphenidate - unii:207zz9qz49) - attention deficit disorders, narcolepsy attention deficit disorders (previously known as minimal brain dysfunction in children). other terms being used to describe the behavioral syndrome below include: hyperkinetic child syndrome, minimal brain damage, minimal cerebral dysfunction, minor cerebral dysfunction. methylphenidate hcl oral solution is indicated as an integral part of a total treatment program which typically includes other remedial measures (psychological, educational, social) for a stabilizing effect in children with a behavioral syndrome characterized by the following group of developmentally inappropriate symptoms: moderate-to-severe distractibility, short attention span, hyperactivity, emotional lability, and impulsivity. the diagnosis of this syndrome should not be made with finality when these symptoms are only of comparatively recent origin. nonlocalizing (soft) neurological signs, learning disability, and abnormal eeg may or may not be present, and a diagnosis of central nervous system dy

Malta - English - Medicines Authority

kern pharma, s.l. polígono industrial colón ii calle venus 72 08228, terrassa, barcelona , spain - film-coated tablet - sitagliptin 50 mg metformin hydrochloride 850 mg - drugs used in diabetes

Malta - English - Medicines Authority

kern pharma, s.l. polígono industrial colón ii calle venus 72 08228, terrassa, barcelona , spain - film-coated tablet - sitagliptin 50 mg metformin hydrochloride 1000 mg - drugs used in diabetes

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

best choice (valu merchandisers company) - tetrahydrozoline hydrochloride (unii: 0yzt43hs7d) (tetrahydrozoline - unii:s9u025y077), zinc sulfate (unii: 89ds0h96tb) (zinc cation - unii:13s1s8sf37) - purposes tetrahydrozoline hcl......redness reliever zinc sulfate......astringent use - for temporary relief of discomfort and redness of the eye due to minor eye irritation

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

heb grocery company., lp - tetrahydrozoline hydrochloride (unii: 0yzt43hs7d) (tetrahydrozoline - unii:s9u025y077), zinc sulfate (unii: 89ds0h96tb) (zinc cation - unii:13s1s8sf37) - purposes tetrahydrozoline hcl......redness reliever zinc sulfate......astringent use - for temporary relief of discomfort and redness of the eye due to minor eye irritation

Egypt - English - EDA (Egyptian Drug Authority)

tiba company for pharmaceutical ind. - topical ointment - 20 %

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

sigma company limited - ascorbic acid,echinacea purpurea,lysine hydrochloride,zinc amino acid chelate -

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

sigma company limited - zinc oxide, quantity: 9.336 mg (equivalent: zinc, qty 7.5 mg); ferrous fumarate, quantity: 15.211 mg (equivalent: iron, qty 5 mg); nicotinamide, quantity: 15 mg; calcium pantothenate, quantity: 10.8 mg; colecalciferol, quantity: 15 microgram; ascorbic acid, quantity: 90 mg; pyridoxine hydrochloride, quantity: 6 mg (equivalent: pyridoxine, qty 4.92 mg); biotin, quantity: 45 microgram; cyanocobalamin, quantity: 20 microgram; folic acid, quantity: 300 microgram; betacarotene, quantity: 1.8 mg; dl-alpha-tocopheryl acetate, quantity: 74.5 mg; heavy magnesium oxide, quantity: 82.919 mg (equivalent: magnesium, qty 50 mg); chromic chloride hexahydrate, quantity: 179.3 microgram (equivalent: chromium, qty 35 microgram); potassium iodide, quantity: 196 microgram (equivalent: iodine, qty 150 microgram); calcium carbonate, quantity: 499.5 mg (equivalent: calcium, qty 200 mg); cupric sulfate pentahydrate, quantity: 3.929 mg (equivalent: copper, qty 1 mg); manganese sulfate monohydrate, quantity: 15.38 mg (equivalent: manganese, qty 5 mg); potassium sulfate, quantity: 178.253 mg (equivalent: potassium, qty 80 mg); riboflavin, quantity: 3.2 mg; thiamine nitrate, quantity: 2.689 mg (equivalent: thiamine, qty 2.18 mg); lutein, quantity: 500 microgram; phytomenadione, quantity: 25 microgram; retinol acetate, quantity: 344.1 microgram (equivalent: vitamin a, qty 300 re); lycopene, quantity: 600 microgram; sodium selenate, quantity: 124.8 microgram (equivalent: selenium, qty 52 microgram) - tablet, film coated - excipient ingredients: maize starch; titanium dioxide; butylated hydroxytoluene; dl-alpha-tocopheryl acetate; sodium ascorbate; sucrose; silicon dioxide; purified water; dl-alpha-tocopherol; starch sodium octenyl succinate; hydrolysed maize starch; croscarmellose sodium; microcrystalline cellulose; maize oil; medium chain triglycerides; sunset yellow fcf aluminium lake; macrogol 400; purified talc; magnesium stearate; colloidal anhydrous silica; maltodextrin; potato starch; hypromellose; butylated hydroxyanisole; gelatin - antioxidant/reduce free radicals formed in the body ; maintain/support energy levels ; maintain/support eye health ; maintain/support general health and wellbeing ; maintain/support bone health ; maintain/support immune system health ; maintain/support absorption of dietary (state vitamin/mineral/nutrient) ; helps prevent dietary (state vitamin/mineral/nutrient) deficiency