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PharmStar Pharmaceuticals
AQUAPRINTM No Other Over the Counter Pain Medication will be as Fast
Acting, Therapeutically Effective, and Safer
AQUAPRINTM Quik-Prin Insta-Prin
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THE COMPANY
PharmStar expects
to be a leader in the pain management field, and to capture a substantial segment of the analgesic, cardio protective, anti-thrombotic
and antipyretic pharmacotherapeutic market, owing to AQUAPRIN and other line extension products significant
competitive advantages. PharmStar's initial base product that has been perfected is AQUAPRIN and INSTA-PRIN. Additional line extension products are now in development.
Aspirin,
(acetylsalicylic acid), is not water soluble and slow to enter the blood stream. Since it is acidic, it causes bleeding
in the digestion track as it is broken down by enzymes. The AQUAPRIN formulation instantly
dissolves aspirin on contact with water making it a, fast-acting, non-acidic, (is antacid), safer, more therapeutically
available, liquid derivative of aspirin. In this form, it virtually eliminates irritation to the GI-tract, and is a more effective and efficient method
of delivering salicylates into the blood stream. This achieves peak blood plasma levels of the drug in 5 to 7 minutes.
Moreover, it contains therapeutically active levels of potassium, which acts also as an antacid in neutralizing stomach
acid. Potassium also lowers blood pressure and helps to dilate blood vessels allowing for better blood circulation.
PharmStar is currently engaged in the validation and setting up of a manufacturing
facility, and continuing product improvements of AQUAPRIN, whose formulation and manufacture depend
mainly upon considerable skill and
"know-how." A
number of patents have been applied for. With new patents applied for, which we feel confident
of being granted in the near future, the Company will enjoy a considerable period of exclusive franchise. . .
AQUAPRIN is already FDA approved and
ready for commercialization. .
The Company is not a “start-up.”
Its founders, since 1993, have continued to perform all the costly research, development and packaging engineering,
product stability, shelf-life testing and quality-control on AQUAPRIN . The product and several line extensions are now ready for scale-up and commercialization. AQUAPRIN will be manufactured in accordance with the current FDA Analgesics Monograph, appearing in the “permitted
combinations” section of the Federal Register and in the USP under the “Effervescent Aspirin” monograph.
It is The Company’s secret intellectual property know-how and long experience in this field that assures investors of
success and no serious competition from others.
The company is headquartered in Rocky Mount, North Carolina. The offices
and research & development space is housed in a 30,000 square foot facility. An additional 170,000 square foot manufacturing
area adjoining the Office and R&D space is available to be used for full scale manufacturing.
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