Singapur - inglés - HSA (Health Sciences Authority)

abbott laboratories (singapore ) private limited - clarithromycin - tablet, film coated - 250 mg - clarithromycin 250 mg

Singapur - inglés - HSA (Health Sciences Authority)

pfizer private limited - horse gamma globulin - injection - 50 mg/ml - horse gamma globulin 50 mg/ml

Singapur - inglés - HSA (Health Sciences Authority)

abbott laboratories (singapore ) private limited - verapamil hydrochloride - tablet, film coated - 240 mg - verapamil hydrochloride 240.0 mg

Malta - inglés - Malta Medicines Authority

alapis s.a. 2 aftokratoros nikolaou street, 17671 athens, greece - timolol, latanoprost - eye drops, solution - timolol 5 mg/ml latanoprost 50 µg/ml - ophthalmologicals

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

stratpharma pty ltd - 62069 - skin semi-occlusive dressing - stratacel is a semi-occlusive wound dressing intended to cover a wound, to provide and support a moist wound environment, and to allow the exchange of gases such as oxygen and water vapor through the device. because stratacel is a gel, it is easily applied to large exposed surface areas and contoured skin, like the face, neck and chest. stratacel can be used with or without a secondary protective dressing. stratacel creates a moist wound environment. stratacel was developed for use as a wound dressing for the repair of damaged or compromised skin following resurfacing procedures such as: ? laser therapy (ablative and non-ablative), including tattoo removal ? dermal abrasion ? chemical peels stratacel may also be used in conjunction with other adjunctive treatments to improve overall results. stratacel contains no alcohols, parabens or fragrances and is transparent and odorless. stratacel is suitable for people with sensitive skin. stratacel may be used during pregnancy and while breastfeeding

Estados Unidos - inglés - NLM (National Library of Medicine)

bayer healthcare pharmaceuticals inc. - iopromide (unii: 712bac33mz) (iopromide - unii:712bac33mz) - iodine 240 mg in 1 ml - ultravist® injection is an iodinated contrast agent indicated for: *for information on the concentrations and doses for the pediatric population [see dosage and administration (2.3) and use in specific populations (8.4)]. risk summary there are no data on ultravist injection use in pregnant women to evaluate for a drug-associated risk of major birth defects, miscarriage, or adverse maternal or fetal outcomes. iopromide crosses the placenta and reaches fetal tissues in small amounts (see data). in animal reproduction studies, intravenous administration of iopromide to pregnant rats and rabbits during organogenesis at doses up to 0.35 and 0.7 times, respectively, the maximum recommended human dose based on body surface area resulted in no relevant adverse developmental effects (see data). . the estimated background risk of major birth defects and miscarriage for the indicated population is unknown. all pregnancies have a background risk of birth defects, loss, or other adverse outcomes. in the u.s. general p

Estados Unidos - inglés - NLM (National Library of Medicine)

physicians total care, inc. - metoprolol tartrate (unii: w5s57y3a5l) (metoprolol - unii:geb06nhm23) - metoprolol tartrate 25 mg - metoprolol tartrate, usp is a selective beta1 -adrenoreceptor blocking agent, available as 25, 50 and 100 mg tablets for oral administration. metoprolol tartrate is (±)-1-(isopropylamino)-3-[p -(2-methoxyethyl)phenoxy]-2-propanol (2:1) dextro -tartrate salt. its structural formula is: metoprolol tartrate is a white, practically odorless, crystalline powder with a molecular weight of 684.82. it is very soluble in water; freely soluble in methylene chloride, in chloroform, and in alcohol; slightly soluble in acetone; and insoluble in ether.   each tablet for oral administration contains 25 mg, 50 mg or 100 mg of metoprolol tartrate.   the tablets contain the following inactive ingredients: microcrystalline cellulose, corn starch, sodium starch glycollate, colloidal silicon dioxide, sodium lauryl sulfate, talc, magnesium stearate, hypromellose, titanium dioxide, polyethylene glycol and polysorbate 80. in addition, 50 mg tablet contains d&c red #30 aluminium lake and 100 mg tablet contains fd&c blu

Estados Unidos - inglés - NLM (National Library of Medicine)

remedyrepack inc. - polymyxin b sulfate (unii: 19371312d4) (polymyxin b - unii:j2vz07j96k), trimethoprim sulfate (unii: e377mf8eq8) (trimethoprim - unii:an164j8y0x) - polymyxin b 10000 [usp'u] in 1 ml - polymyxin b sulfate and trimethoprim ophthalmic solution, usp is a sterile antimicrobial solution for topical ophthalmic use. it has ph of 4.0 to 5.5 and osmolality of 270 to 310 mosm/kg. chemical names: trimethoprim sulfate, 2,4-diamino-5-(3,4,5-trimethoxybenzyl) pyrimidine sulfate, is a white, odorless, crystalline powder with a molecular weight of 678.72 and the following structural formula: c 28 h 38 n 8 o 10 s mol. wt. 678.72 polymyxin b sulfate is the sulfate salt of polymyxin b 1 and b 2 which are produced by the growth of bacillus polymyxa  (prazmowski) migula (fam. bacillaceae). it has a potency of not less than 6,000 polymyxin b units per mg, calculated on an anhydrous basis. the structural formula is: each ml contains: actives: polymyxin b sulfate equal to 10,000 polymyxin b units, trimethoprim sulfate (equivalent to trimethoprim 1 mg); inactives: purified water, sodium chloride. sulfuric acid and, if necessary, sodium hydroxide may be added to adjust ph (4.0 – 5.5). preservative: benzalkonium chloride 0.004%

Estados Unidos - inglés - NLM (National Library of Medicine)

stat rx usa llc - methylphenidate hydrochloride (unii: 4b3sc438hi) (methylphenidate - unii:207zz9qz49) - methylphenidate hydrochloride 5 mg - description methylphenidate hydrochloride usp, is a mild central nervous system (cns) stimulant, available as tablets of 5, 10, and 20 mg for oral administration. methylphenidate hydrochloride is methyl α-phenyl-2-piperidineacetate hydrochloride, and its structural formula is      methylphenidate 5mg structure image methylphenidate hydrochloride usp is a white, odorless, fine crystalline powder. its solutions are acid to litmus. it is freely soluble in water and in methanol, soluble in alcohol, and slightly soluble in chloroform and in acetone. its molecular formula is c14 h19 no2 •hcl, and its molecular weight is 269.77. inactive ingredients. methylphenidate hydrochloride tablets: colloidal silicon dioxide, compressible sugar, lactose monohydrate and magnesium stearate. additionally, the 5 mg contains fd and c blue #2 and fd and c red #40; the 10 mg contains fd and c blue #2 and d and c yellow #10; and the 20 mg contains fd and c yellow #6. methylphenidate is a mild central nervous system stimula

Estados Unidos - inglés - NLM (National Library of Medicine)

elanco us inc. - desoxycorticosterone pivalate (unii: 16665t4a2x) (desoxycortone - unii:40gp35yq49) - desoxycorticosterone pivalate 25 mg in 1 ml - the active ingredient in percorten-v is desoxycorticosterone pivalate (docp). it is a mineralocorticoid hormone and an analog of desoxycorticosterone. it is white, odorless, and stable in air. it is practically insoluble in water, sparingly soluble in acetone, slightly soluble in methanol, ether and vegetable oils. the molecular weight is 414.58. it is designated chemically as 21 (2,2-dimethyl-1-oxopropoxy)-pregn-4-ene-3,20-dione. the empirical formula is c26 h38 o4 and the structural formula is: percorten-v is a white aqueous suspension. each ml contains 25mg desoxycorticosterone pivalate, 10.5mg methylcellulose, 3mg sodium carboxymethylcellulose, 1mg polysorbate 80 and 8mg sodium chloride with 0.002% thimerosal as preservative in water for injection.