ANTIMICROBIAL HAND- triclosan soap United States - English - NLM (National Library of Medicine)

antimicrobial hand- triclosan soap

mckesson medical-surgical inc. - triclosan (unii: 4nm5039y5x) (triclosan - unii:4nm5039y5x) - triclosan 0.375 g in 100 ml - mckesson antimicrobial soap clean scent | with pump net contents 18 oz (532 ml) - uses - an effective antimicrobial hand cleanser. - kills and inhibits bacterial growth on hands. - gentle cleansers leave hands clean and moisturized. - reduces the possibility of cross-contamination.

McKesson Lansoprazole Delayed-Release Capsules 15 mg Drug Facts United States - English - NLM (National Library of Medicine)

mckesson lansoprazole delayed-release capsules 15 mg drug facts

strategic sourcing services llc - lansoprazole (unii: 0k5c5t2qpg) (lansoprazole - unii:0k5c5t2qpg) - acid reducer

McKesson Calcium Antacid Drug Facts United States - English - NLM (National Library of Medicine)

mckesson calcium antacid drug facts

strategic sourcing services llc - calcium carbonate (unii: h0g9379fgk) (calcium cation - unii:2m83c4r6zb, carbonate ion - unii:7ujq5ope7d) - antacid relieves presently taking a prescription drug. antacids may interact with certain prescription drugs.

MCKESSON ANTIBACTERIAL SOAP SOLUTION Canada - English - Health Canada

mckesson antibacterial soap solution

central solutions inc. - benzethonium chloride - solution - 0.13% - benzethonium chloride 0.13%

MCKESSON FOAMING ANTIBACTERIAL SOAP SOLUTION Canada - English - Health Canada

mckesson foaming antibacterial soap solution

central solutions inc. - benzethonium chloride - solution - 0.13% - benzethonium chloride 0.13%

FUROSEMIDE- furosemide tablet United States - English - NLM (National Library of Medicine)

furosemide- furosemide tablet

mckesson corporation dba sky packaging - furosemide (unii: 7lxu5n7zo5) (furosemide - unii:7lxu5n7zo5) - furosemide 20 mg - furosemide tablets, usp is indicated in adults and pediatric patients for the treatment of edema associated with congestive heart failure, cirrhosis of the liver, and renal disease, including the nephrotic syndrome. furosemide is particularly useful when an agent with greater diuretic potential is desired. furosemide tablets, usp may be used in adults for the treatment of hypertension alone or in combination with other antihypertensive agents. hypertensive patients who cannot be adequately controlled with thiazides will probably also not be adequately controlled with furosemide alone. furosemide tablets are contraindicated in patients with anuria and in patients with a history of hypersensitivity to furosemide.

LAMOTRIGINE - lamotrigine tablet 
LAMOTRIGINE- lamotrigine tablet United States - English - NLM (National Library of Medicine)

lamotrigine - lamotrigine tablet lamotrigine- lamotrigine tablet

mckesson corporation dba sky packaging - lamotrigine (unii: u3h27498ks) (lamotrigine - unii:u3h27498ks) - lamotrigine 100 mg - adjunctive therapy lamotrigine tablets are indicated as adjunctive therapy for the following seizure types in patients aged 2 years and older: - partial-onset seizures. - primary generalized tonic-clonic (pgtc) seizures. - generalized seizures of lennox-gastaut syndrome. monotherapy lamotrigine tablets are indicated for conversion to monotherapy in adults (aged 16 years and older) with partial-onset seizures who are receiving treatment with carbamazepine, phenytoin, phenobarbital, primidone, or valproate as the single antiepileptic drug (aed). safety and effectiveness of lamotrigine tablets have not been established (1) as initial monotherapy; (2) for conversion to monotherapy from aeds other than carbamazepine, phenytoin, phenobarbital, primidone, or valproate; or (3) for simultaneous conversion to monotherapy from 2 or more concomitant aeds. lamotrigine tablets are indicated for the maintenance treatment of bipolar i disorder to delay the time to occurrence of mood episodes (depression, mania, hypoman

GALANTAMINE tablet, film coated United States - English - NLM (National Library of Medicine)

galantamine tablet, film coated

mckesson corporation dba sky packaging - galantamine hydrobromide (unii: mj4ptd2vvw) (galantamine - unii:0d3q044kca) - galantamine 8 mg - galantamine tablets are indicated for the treatment of mild to moderate dementia of the alzheimer’s type. galantamine tablets are contraindicated in patients with known hypersensitivity to galantamine hydrobromide or to any excipients used in the formulation. teratogenic effects pregnancy category c: there are no adequate and well-controlled studies in pregnant women. in studies conducted in animals, administration of galantamine during pregnancy resulted in developmental toxicity (increased incidence of morphological abnormalities and decreased growth in offspring) at doses similar to or greater than those used clinically. galantamine hydrobromide should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. in rats, administration of galantamine (oral doses of 2, 8, or 16 mg/kg/day), from day 14 (females) or day 60 (males) prior to mating and continuing in females through the period of organogenesis, resulted in an increased incidence of fetal skeletal

DONEPEZIL HYDROCHLORIDE- donepezil hydrochloride tablet United States - English - NLM (National Library of Medicine)

donepezil hydrochloride- donepezil hydrochloride tablet

mckesson corporation dba sky packaging - donepezil hydrochloride (unii: 3o2t2pj89d) (donepezil - unii:8ssc91326p) - donepezil hydrochloride 5 mg - donepezil hydrochloride tablets are indicated for the treatment of dementia of the alzheimer's type. efficacy has been demonstrated in patients with mild, moderate, and severe alzheimer's disease. donepezil hydrochloride is contraindicated in patients with known hypersensitivity to donepezil hydrochloride or to piperidine derivatives. risk summary there are no adequate data on the developmental risks associated with the use of donepezil hydrochloride in pregnant women. in animal studies, developmental toxicity was not observed when donepezil was administered to pregnant rats and rabbits during organogenesis, but administration to rats during the latter part of pregnancy and throughout lactation resulted in increased stillbirths and decreased offspring survival at clinically relevant doses [see data ]. in the u.s. general population, the estimated background risks of major birth defects and miscarriage in clinically recognized pregnancies are 2% to 4% and 15% to 20%, respectively. the background risks of major

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

prednisone tablet

mckesson corporation dba sky packaging - prednisone (unii: vb0r961hzt) (prednisone - unii:vb0r961hzt) - prednisone 5 mg - prednisone tablets are indicated in the following conditions: - endocrine disorders primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance) congenital adrenal hyperplasia nonsuppurative thyroiditis hypercalcemia associated with cancer primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the first choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy mineralocorticoid supplementation is of particular importance) congenital adrenal hyperplasia nonsuppurative thyroiditis hypercalcemia associated with