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Bupropion

Bupropion (INN; previously known as amfebutamone, Wellbutrin, Zyban) is an atypical antidepressant that acts as a norepinephrine and dopamine reuptake inhibitor, and nicotinic antagonist. Bupropion belongs to the chemical class of aminoketones and is similar in structure to the stimulant cathinone, to the anorectic diethylpropion, and to phenethylamines in general.

- Bupropion Hydrochloride
- Carbidopa
- Diltiazem
- Diltiazem HCl
- Fosphenytoin
- Fosphenytoin Sodium
- Levetiracetam
- Loratadine
- Naproxen
- Niacin
- Phenylephrine HCl
- Risedronate Sodium
- Sibutramine HCl Monohydrate
- Tamsulosin
- Tamsulosin Chloride
- Triprolidine
- Verapamil
- Verapamil Hydrochloride
- Zolpidem Tartrate
- Bupropion HCL
- Deslortadine
- Dextromethorphan
- Diltiazem Chloride
- Gabapentin
- Iopamidol
- Levodopa
- Nabumetone
- Naproxen Sodium
- Phenylephrine
- Phenylephrine Hydrochloride
- Sibutramine
- Sibutramine Chloride Monohydrate
- Tamsulosin HCl
- Triprolidine Hydrochloride
- Triprolidine HCl
- Verapamil HCl
- Zolpidem


  Naproxen

Naproxen (INN) (pronounced /n'prksn/) is a non-steroidal anti-inflammatory drug (NSAID) commonly used for the reduction of moderate to severe pain, fever, inflammation and stiffness caused by conditions such as osteoarthritis, rheumatoid arthritis, psoriatic arthritis, gout, ankylosing spondylitis, injury (like fractures), menstrual cramps, tendinitis, bursitis, and the treatment of primary dysmenorrhea. It works by inhibiting both the COX-1 and COX-2 enzymes. Naproxen and naproxen sodium are marketed under various trade names including: Aleve, Anaprox, Miranax, Naprogesic, Naprosyn, Naprelan, Synflex.



  Naproxen Sodium

Naproxen was first and originally marketed as the prescription drug Naprosyn in 1976 and naproxen sodium was first marketed under the trade name Anaprox in 1980. It remains a prescription-only drug in much of the world. The U.S. Food and Drug Administration (FDA) approved the use of naproxen sodium as an over-the-counter (OTC) drug in 1994, where OTC preparations are sold under the trade name Aleve. In Australia, small packets of lower-strength preparations of naproxen sodium are Schedule 2 Pharmacy Medicines.



  Niacin

Niacin, also known as nicotinic acid and vitamin B3, is the organic compound with the formula HO2CC5H4N. This water-soluble, colorless solid is a derivative of pyridine, featuring a carboxylic acid functional group at the 3-position. The designation vitamin B3 also includes the corresponding amide nicotinamide ("niacinamide"), wherein the CO2H group has been replaced by a CONH2 group. Niacin is a precursor to NADH, NAD, NAD+, and NADP, which play essential metabolic roles in living cells. Among its many functions, niacin derivatives are involved with detoxification of xenochemicals, DNA repair, and the production of steroid hormones in the adrenal gland.



  Phenylephrine

Phenylephrine is used as a decongestant, available as an oral medicine or as a nasal spray. Phenylephrine is now the most common over-the-counter (OTC) decongestant; oxymetazoline is a more common nasal spray.[citation needed] Pseudoephedrine was historically more common, although its notoriety as a precursor has led some governments to restrict its sale.


  Phenylephrine HCl

Phenylephrine or Neo-Synephrine is an a-adrenergic receptor agonist used primarily as a decongestant, as an agent to dilate the pupil and to increase blood pressure. Phenylephrine has recently been marketed as a substitute for pseudoephedrine, (e.g. Pfizer's Sudafed (Original Formulation)) but there are recent claims that oral phenylephrine may be no more effective as a decongestant than placebo



  Phenylephrine Hydrochloride

Oral phenylephrine is extensively metabolised by monoamine oxidase [1], an enzyme which is present in the gastrointestinal tract and the liver. Therefore, compared to orally-taken pseudoephedrine, it has a reduced and variable bioavailability of only up to 38 percent [2][3], and is therefore less effective as a nasal decongestant than pseudoephedrine. Because phenylephrine is a direct selective a-adrenergic receptor agonist, it does not cause the release of endogenous noradrenaline like pseudoephedrine does. Therefore, phenylephrine is less likely to cause side-effects like central nervous system stimulation, insomnia, anxiety, irritability and restlessness.



  Risedronate Sodium

FDA informed healthcare professionals and patients of the possibility of severe and sometimes incapacitating bone, joint, and/or muscle (musculoskeletal) pain in patients taking bisphosphonates. Although severe musculoskeletal pain is included in the prescribing information for all bisphosphonates, the association between bisphosphonates and severe musculoskeletal pain may be overlooked by healthcare professionals, delaying diagnosis, prolonging pain and/or impairment, and necessitating the use of analgesics. The severe musculoskeletal pain may occur within days, months, or years after starting a bisphosphonates. Some patients have reported complete relief of symptoms after discontinuing the bisphosphonate, whereas others have reported slow or incomplete resolution. The risk factors for and incidence of severe musculoskeletal pain associated with bisphosphonates are unknown



  Sibutramine

Sibutramine (trade name Meridia in the USA, Reductil in Europe and other countries), usually as sibutramide hydrochloride monohydrate, is an orally administered agent for the treatment of obesity. It is a centrally-acting serotonin-norepinephrine reuptake inhibitor structurally related to amphetamines,[1] although its mechanism of action is distinct.Sibutramine is manufactured by Abbott Laboratories. It is classified as a Schedule IV controlled substance in the United States.



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