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Packaging Type | Bottle |
Dose/Strength (ex. 1 mg or 1 ml) | 1mg/ml |
Packaging Size | 10 ml |
Usage | Clinical, Hospital |
Form | Injection |
Dose type | Allopathic |
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Dose/Strength (ex. 1 mg or 1 ml) | 0.5 ml |
Type | Anti - rabies vaccine |
Packaging Type | Bottle |
Packaging Size | 100 ml |
Dosage Form | Injection |
Usage | Clinical, Hospital |
Composition per single dose:
The Neomycin, Kanamycin and Polymyxin - B sulphate used in the cell and virus cultures are eliminated to the greatest extent during purification procedures and cannot be detected in the final vaccine.
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Packaging Type | Bottle |
Dose/Strength (ex. 1 mg or 1 ml) | 10 ml |
Packaging Size | 100 ml |
Usage | Clinical, Hospital |
Form | Injection |
Type | Vaccination |
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Packaging Type | Bottle |
Dose/Strength (ex. 1 mg or 1 ml) | 5mg/ml |
Form | Injection |
Packaging Size | 100 ml |
Usage | Hospital, Clinical |
Drug name | Meningitis |
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Dose | 1ml-5ml |
Packaging Type | Glass Bottle |
Injectable Form | Solution |
Application | Analgesics and Pain Relief Medicines, Anti Infective & Common Disease Medicines |
Injection Site | Intramuscular |
Medicine Type | Allopathic |
Packaging Size | 100 ml |
Usage | Clinical, Hospital |
Almost all (97%) children between age 12 months and 12 years develop immunity to the disease after one dose of vaccine. For older children and adults, an average of 78% develop immunity after one dose and 99% develop immunity after the recommended two doses.
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Oral Polio Vaccines (OPV) consists of a mixture of live attenuated poliovirus strains of each of the three serotypes, selected by their ability to mimic the immune response following infection with wild polioviruses, but with a significantly reduced incidence of spreading to the central nervous system.*Your information is safe with us.
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Packaging Type | Bottle |
Dose/Strength (ex. 1 mg or 1 ml) | 5mg/ml |
Packaging Size | 100 ml |
Usage | Clinical, Hospital |
Generic Name | MMR |
Form | Injection |
The vaccine is a mixture of three live attenuated viruses, administered via injection. The shot is generally administered to children around the age of one year, with a second dose before starting school (i.e. age 4/5). The second dose is a dose to produce immunity in the small number of persons (2–5%) who fail to develop measles immunity after the first dose. In the United States, the vaccine was licensed in 1971 and the second dose was introduced in 1989. It is widely used around the world; since introduction of its earliest versions in the 1970s, over 500 million doses have been used in over 60 countries. As with all vaccinations, long-term effects and efficacy are subject to continuing study. The vaccine is sold by Merck as M-M-R II, Glaxo SmithKline Biologicals as Priorix, Serum Institute of India as Tresivac and Sanofi Pasteur as Trimovax.
It is usually considered a childhood vaccination. However, it is also recommended for use in some cases of adults with HIV.
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Grade Standard | Analytical Grade, Reagent Grade |
Physical State | Liquid |
Usage | Commerical, Laboratory |
Packaging Type | Bottle |
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Being the highly acclaimed stockiest and leading supplier of life saving vaccines, we stock serum’s T.D.Vaccines which is the heavily consumed vaccine to prevent from diphtheria and peruses diseases. This vaccine is especially manufactured for adults to protect them from fatal diseases and is able to achieve international standards. We made these vaccines available at very low costs in the market.*Your information is safe with us.
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DPT (also DTP and DTwP) refers to a class of combination vaccines against three infectious diseases in humans: diphtheria, pertussis (whooping cough) andtetanus. The vaccine components include diphtheria and tetanus toxoids, and killed whole cells of the organism that causes pertussis (wP).
DTaP and Tdap refer to similar combination vaccines in which the pertussis component is acellular.
Also available is the DT or TD vaccine, which lacks the pertussis component.
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