NALOXONE HYDROCHLORIDE- nalxone hydrochloride injection United States - English - NLM (National Library of Medicine)

naloxone hydrochloride- nalxone hydrochloride injection

medical purchasing solutions, llc - naloxone hydrochloride (unii: f850569pqr) (naloxone - unii:36b82amq7n) - naloxone hydrochloride injection, usp is indicated for the complete or partial reversal of opioid depression, including respiratory depression, induced by natural and synthetic opioids, including propoxyphene, methadone, and certain mixed agonist-antagonist analgesics: nalbuphine, pentazocine, butorphanol, and cyclazocine. naloxone hydrochloride injection, usp is also indicated for diagnosis of suspected or known acute opioid overdosage. naloxone hydrochloride injection, usp may be useful as an adjunctive agent to increase blood pressure in the management of septic shock (see clinical pharmacology; adjunctive use in septic shock ). naloxone hydrochloride injection is contraindicated in patients known to be hypersensitive to naloxone hydrochloride or to any of the other ingredients in naloxone hydrochloride injection. naloxone hydrochloride injection is an opioid antagonist. physical dependence associated with the use of naloxone hydrochloride injection has not been reported. tolerance to the opio

Naloxone Hydrochloride Minijet 400 micrograms/ml Solution for injection Ireland - English - HPRA (Health Products Regulatory Authority)

naloxone hydrochloride minijet 400 micrograms/ml solution for injection

dlrc pharma services limited - naloxone hydrochloride - solution for injection - 400 microgram(s)/millilitre - antidotes; naloxone

NALOXONE HYDROCHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

naloxone hydrochloride injection, solution

mylan institutional llc - naloxone hydrochloride (unii: f850569pqr) (naloxone - unii:36b82amq7n) - naloxone hydrochloride injection is indicated for the complete or partial reversal of opioid depression, including respiratory depression, induced by natural and synthetic opioids including propoxyphene, methadone, and certain mixed agonist-antagonist analgesics: nalbuphine, pentazocine, butorphanol and cyclazocine. naloxone hydrochloride injection is also indicated for diagnosis of suspected or known acute opioid overdosage. naloxone hydrochloride injection may be useful as an adjunctive agent to increase blood pressure in the management of septic shock (see clinical pharmacology: adjunctive use in septic shock). naloxone hydrochloride injection is contraindicated in patients known to be hypersensitive to naloxone hydrochloride or to any of the other ingredients contained in the formulation. naloxone hydrochloride injection is an opioid antagonist. physical dependence associated with the use of naloxone hydrochloride injection has not been reported. tolerance to the opioid antagonist effect of naloxone is no

NALOXONE HYDROCHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

naloxone hydrochloride injection, solution

hf acquisition co llc, dba healthfirst - naloxone hydrochloride (unii: f850569pqr) (naloxone - unii:36b82amq7n) - naloxone hydrochloride injection is indicated for the complete or partial reversal of opioid depression, including respiratory depression, induced by natural and synthetic opioids including propoxyphene, methadone, and certain mixed agonist-antagonist analgesics: nalbuphine, pentazocine, butorphanol and cyclazocine. naloxone hydrochloride is also indicated for the diagnosis of suspected or known acute opioid overdosage. naloxone may be useful as an adjunctive agent to increase blood pressure in the management of septic shock (see clinical pharmacology, adjunctive use in septic shock). naloxone hydrochloride injection is contraindicated in patients known to be hypersensitive to naloxone hydrochloride or to any of the other ingredients contained in the formulation. naloxone hydrochloride injection is an opioid antagonist. physical dependence associated with the use of naloxone hydrochloride injection has not been reported. tolerance to the opioid antagonist effect of naloxone is not known to occur.

NALOXONE HYDROCHLORIDE injection, solution United States - English - NLM (National Library of Medicine)

naloxone hydrochloride injection, solution

eugia us llc - naloxone hydrochloride (unii: f850569pqr) (naloxone - unii:36b82amq7n) - naloxone hydrochloride injection is indicated for the complete or partial reversal of opioid depression, including respiratory depression, induced by natural and synthetic opioids, including propoxyphene, methadone and certain mixed agonist-antagonist analgesics: nalbuphine, pentazocine, butorphanol, and cyclazocine. naloxone hydrochloride injection is also indicated for diagnosis of suspected or known acute opioid overdosage. naloxone hydrochloride injection may be useful as an adjunctive agent to increase blood pressure in the management of septic shock (see clinical pharmacology; adjunctive use in septic shock ). naloxone hydrochloride injection is contraindicated in patients known to be hypersensitive to naloxone hydrochloride or to any of the other ingredients contained in the formulation. naloxone hydrochloride is an opioid antagonist. physical dependence associated with the use of naloxone hydrochloride has not been reported. tolerance to the opioid antagonist effect of naloxone hydrochloride is n

Moxonidine EG 0.4 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

moxonidine eg 0.4 mg film-coat. tabl.

eg sa-nv - moxonidine 0,4 mg - film-coated tablet - 0,4 mg - moxonidine 0.4 mg - moxonidine

Moxonidine EG 0.2 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

moxonidine eg 0.2 mg film-coat. tabl.

eg sa-nv - moxonidine 0,2 mg - film-coated tablet - 0,2 mg - moxonidine 0.2 mg - moxonidine

Moxonidine Viatris 0.2 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

moxonidine viatris 0.2 mg film-coat. tabl.

viatris gx bv-srl - moxonidine 0,2 mg - film-coated tablet - 0,2 mg - moxonidine 0.2 mg - moxonidine

Moxonidine Viatris 0.4 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

moxonidine viatris 0.4 mg film-coat. tabl.

viatris gx bv-srl - moxonidine 0,4 mg - film-coated tablet - 0,4 mg - moxonidine 0.4 mg - moxonidine

Moxonidine Viatris 0.3 mg film-coat. tabl. Belgium - English - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

moxonidine viatris 0.3 mg film-coat. tabl.

viatris gx bv-srl - moxonidine 0,3 mg - film-coated tablet - 0,3 mg - moxonidine 0.3 mg - moxonidine