ACETYLCYSTEINE SOLUTION USP Kanāda - angļu - Health Canada

acetylcysteine solution usp

sterimax inc - acetylcysteine - solution - 200mg - acetylcysteine 200mg

NALTREXONE HYDROCHLORIDE tablet, film coated Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

naltrexone hydrochloride tablet, film coated

tagi pharma inc. - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride 50 mg - naltrexone hydrochloride tablets usp are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. naltrexone hydrochloride tablets usp have not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions. naltrexone hydrochloride is contraindicated in: - patients receiving opioid analgesics. - patients currently dependent on opioids, including those currently maintained on opiate agonists (e.g., methadone) or partial agonists (e.g., buprenorphine). - patients in acute opioid withdrawal (see warnings ). - any individual who has failed the naloxone challenge test or who has a positive urine screen for opioids. - any individual with a history of sensitivity to naltrexone hydrochloride or any other components of this product. it is not known if there is any cross-sensitivity with naloxone or the phenanthrene containing opioids. naltrexone hydrochloride is a pure opioid antagonist. it does not

NALTREXONE HYDROCHLORIDE tablet, film coated Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

naltrexone hydrochloride tablet, film coated

physicians total care, inc. - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride 50 mg - naltrexone hydrochloride tablets are indicated in the treatment of alcohol dependence and for the blockade of the effects of exogenously administered opioids. naltrexone has not been shown to provide any therapeutic benefit except as part of an appropriate plan of management for the addictions. naltrexone is contraindicated in: - patients receiving opioid analgesics. - patients currently dependent on opioids, including those currently maintained on opiate agonists (e.g., methadone or laam (levo-alpha-acetyl-methadol). - patients in acute opioid withdrawal (see warnings). - any individual who has failed the naloxone challenge test or who has a positive urine screen for opioids. - any individual with a history of sensitivity to naltrexone or any other components of this product. it is not known if there is any cross-sensitivity with naloxone or the phenanthrene containing opioids. - any individual with acute hepatitis or liver failure. naltrexone is a pure opioid antagonist. it does not lead to physical or psyc

NALTREXONE GH naltrexone hydrochloride 50mg film coated tablets blister pack Austrālija - angļu - Department of Health (Therapeutic Goods Administration)

naltrexone gh naltrexone hydrochloride 50mg film coated tablets blister pack

generic health pty ltd - naltrexone hydrochloride, quantity: 50 mg - tablet, film coated - excipient ingredients: titanium dioxide; powdered cellulose; lactose monohydrate; microcrystalline cellulose; iron oxide black; crospovidone; iron oxide yellow; colloidal anhydrous silica; iron oxide red; hypromellose; macrogol 4000; magnesium stearate - naltrexone gh is indicated for use within a comprehensive treatment programme for alcohol dependence. naltrexone gh is also indicated as adjunctive therapy in the maintenance of formerly opioid-dependent patients who have ceased the use of opioids such as diamorphine (heroin) and morphine.

Naltrexone Hydrochloride Tablet, film coated 50mg Malta - angļu - Medicines Authority

naltrexone hydrochloride tablet, film coated 50mg

accord healthcare limited - naltrexone hydrochloride - film-coated tablet - naltrexone hydrochloride 50 mg - other nervous system drugs

Naltrexone Hydrochloride 50mg film-coated Tablet Malta - angļu - Medicines Authority

naltrexone hydrochloride 50mg film-coated tablet

accord healthcare ireland ltd euro house, euro business park, little island cork, t45 k857, ireland - naltrexone hydrochloride - film-coated tablet - naltrexone hydrochloride 50 mg - other nervous system drugs

NALTREXONE HYDROCHLORIDE tablet film coated Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

naltrexone hydrochloride tablet film coated

avera mckennan hospital - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride 50 mg

Naltrexone 50 mg film-coated tablets Īrija - angļu - HPRA (Health Products Regulatory Authority)

naltrexone 50 mg film-coated tablets

aop orphan pharmaceuticals gmbh - naltrexone hydrochloride - film-coated tablet - 50 milligram(s) - drugs used in alcohol dependence; naltrexone

NALTREXONE HYDROCHLORIDE tablet film coated Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

naltrexone hydrochloride tablet film coated

pd-rx pharmaceuticals, inc. - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride 50 mg

NALTREXONE HYDROCHLORIDE tablet film coated Amerikas Savienotās Valstis - angļu - NLM (National Library of Medicine)

naltrexone hydrochloride tablet film coated

bryant ranch prepack - naltrexone hydrochloride (unii: z6375yw9sf) (naltrexone - unii:5s6w795cqm) - naltrexone hydrochloride 50 mg