Dextropropoxyphene plus Paracetamol 32.5 mg (Darvon)

Dextropropoxyphene plus Paracetamol 32.5 mg (Darvon)

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buy Darvon online

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Description
Description Dextropropoxyphene is an analgesic in the opioid category, patented in 1955 and manufactured by Eli Lilly and Company. It is an optical isomer of levopropoxyphene. It is intended to treat mild pain and also has antitussive and local anaesthetic effects.
Formula: C22H29NO2
Molar mass: 339.471 g/mol
CAS ID: 469-62-5
Elimination half-life: 6–12 hours; 30–36 hours (active metabolite, nordextropropoxyphene)
ATC code: N02AC04 (WHO)
Melting point: 75 °C (167 °F)
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Buy Dextropropoxyphene Online from Chemicals Pharm Store.

 

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Description Dextropropoxyphene is an analgesic in the opioid category, patented in 1955 and manufactured by Eli Lilly and Company. It is an optical isomer of levopropoxyphene. It is intended to treat mild pain and also has antitussive and local anaesthetic effects.
Formula: C22H29NO2
Molar mass: 339.471 g/mol
CAS ID: 469-62-5
Elimination half-life: 6–12 hours; 30–36 hours (active metabolite, nordextropropoxyphene)
ATC code: N02AC04 (WHO)
Melting point: 75 °C (167 °F)
People also search for: Pethidine, Phencyclidine, Methaqualone,

Buy Darvon Online / Order Darvon Wholesale  / Retail Supplies Usage.

Best place to buy Dextropropoxyphene  Online is a narcotic analgesic structurally related to METHADONE. Only the dextro-isomer has an analgesic effect; the levo-isomer appears to exert an antitussive effect.

Propoxyphene is an Opioid Agonist. The mechanism of action of propoxyphene is as a Full Opioid Agonist.

High Quality Darvon Online History .

Where can i buy  Dextropropoxyphene  Online? Propoxyphene is the d-isomer of synthetic diphenyl propionate derivative propoxyphene, with narcotic analgesic effect. This agent mimics the effects of the endogenous opiate dextropropoxyphene, by binding to mu receptors located throughout the central nervous system. The binding results in GTP to GDP exchanges on the mu-G-protein complex, by which effector adenylate cyclase is inactivated thereby decreasing intracellular cAMP. This, in turn, inhibits the release of various nociceptive neurotransmitters, such as substance P, gamma-aminobutyric acid (GABA), dopamine, acetylcholine, noradrenaline, vasopressin, and somatostatin. In addition, dextropropoxyphene closes N-type voltage-gated calcium channels and opens calcium-dependent inwardly rectifying potassium channels. This results in hyperpolarization, thereby reducing neuronal excitability, which further decreases the perception of pain.

Why is Darvon banned?

REASONS FOR WITHDRAWAL OF DEXTROPROPOXYPHENE

The reasons cited for its withdrawal from these countries include its implication in overdose related deaths and its impact on cardiovascular electrophysiology even within therapeutic dose range. Additionally, concerns have been expressed about its utility as an analgesic.

What is dextropropoxyphene used for?
Dextropropoxyphene is an analgesic in the opioid category, patented in 1955 and manufactured by Eli Lilly and Company. It is an optical isomer of levopropoxyphene. It is intended to treat mild pain and also has antitussive (cough suppressant) and local anaesthetic effects.
What is the brand name for propoxyphene?
Darvocet (propoxyphene and acetaminophen) is a combination of a narcotic pain reliever and a less potent pain reliever and a fever reducer used for the treatment of mild to moderate pain. The brand name Darvocet is no longer available in the U.S. Generic versions may be available.

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