Pharmaceutical Benzydamine Hcl Powder Raw Materials CAS 111470-99-6 API Factory Supply
Pharmaceutical Benzydamine Hcl Powder Raw Materials CAS 111470-99-6 API Factory Supply
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Pharmaceutical Benzydamine Hcl Powder Raw Materials CAS 111470-99-6 API Factory Supply

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Benzydamine Hcl Powder Usage and Synthesis.

Benzydamine Hydrochloride. This product is a non-specific anti-inflammatory drugs, anti-inflammatory, antipyretic, analgesic effect.Benzydamine Hcl Powder is effective for pain caused by inflammation.Benzydamine Hcl Raw Materials also has an antispasmodic effect. 

Commonly used in surgery and trauma caused by a variety of inflammation and arthritis, bronchitis, pharyngitis. Can be combined with antibacterial agents or sulfonamides for better efficacy.

Benzydamine Hcl Powder

Uses and functions of Benzydamine Hcl Powder.

It is a non-specific anti-inflammatory drug with anti-inflammatory, antipyretic and analgesic effects. It is effective for pain caused by inflammation. The anti-inflammatory effect is similar to or slightly stronger than that of POTASONE. 

This product also has antispasmodic effect. Commonly used in surgery and trauma caused by a variety of inflammation and arthritis, bronchitis, pharyngitis. Can be combined with antibacterial agents or sulfonamides for better efficacy.

Benzydamine Hcl Powder

Pharmacological Effects of Benzydamine Hcl Powder.

Benzydamine is structurally unrelated to corticosteroids.The action of benzydamine can be mediated by the prostaglandin system.

The drug may affect thromboxane formation and alter prostaglandin biosynthesis, and the desired dose can be achieved with topical administration.Benzydamine shows stabilising effects on cell membranes, inhibits degranulation of human neutrophils, and inhibits platelet aggregation.

Benzydamine may affect tissue biochemistry related to local mechanisms of inflammation and pain.

Benzydamine Hcl Powder

Production method of Benzydamine Hcl Powder.

a), according to the above proportion of benzydamine hydrochloride with a concentration of 80% ethanol aqueous solution of soft material, through 20 mesh sieve granulation, at 60 ~ 70 ℃ ventilation drying 1 hour;

b), pass the above dried granules through a 30-mesh sieve to make a whole granule, and then add sodium chloride, cross-linked sodium carboxymethyl cellulose, sodium dodecyl sulfate and leucine in the above proportion in turn, and mix well;

c), determine the content of the above mixture, calculate the weight of the tablet, and press the tablet to obtain the finished product.


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