High-Quality Aspirin Tablets with GMP/BP/USP Supplier, Products

[Drug name]
Common name: Aspirin tablets
Trade name: Aspirin tablets
English name: Aspirin Tablets

[Composition and traits]
Main ingredients: The main ingredient of this product is aspirin.
Character: This product is a white piece.

[indication]
This product is suitable for inhibiting platelet aggregation, reducing myocardial infarction, temporary cerebral ischemia or stroke incidence in atherosclerosis patients.

[Specifications and Packaging]
Single-dose specification: 500MG
Packaging specification: 10x5 pieces

[usage and dosage]
profess to be convinced. The daily dose is approximately 50-150mg, taken once or twice, or as prescribed.

[untoward effect]
Daily doses over 1000mg may cause upper abdominal discomfort, nausea, vomiting, stomachache, and occasionally a mild increase in systolic and diastolic blood pressure or a mild increase in Bun and serum creatinine values.

[taboo]
1. Those allergic to this product are prohibited.
2. Patients with gastrointestinal ulcerdisease or other active bleeding, hemophilia or thrombocytopenia are prohibited.

[matters need attention]
1. Use with caution in the allergic history of salicylic acid drugs or non-steroidal anti-inflammatory drugs.
2. Use with caution in pregnant women, especially those in the last trimester of pregnancy and lactating women.

[condition of storage]
Keep sealed below 25℃.

[term of validity]
24 Months

Product Description

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Premium Pharmaceutical Standards
All products are manufactured under strict GMP compliance to ensure the highest safety and efficacy for global distribution.
Frequently Asked Questions
1. What do GMP, BP, and USP standards signify?
GMP (Good Manufacturing Practice), BP (British Pharmacopoeia), and USP (United States Pharmacopeia) are international quality standards that ensure pharmaceutical products are consistently produced and controlled according to strict quality regulations.
2. How are the liquid injections packaged for safe transport?
Our injections are sealed in medical-grade glass ampoules or vials and secured in protective inner trays and reinforced export cartons to prevent breakage and maintain sterility during transit.
3. Can these products be registered in my country?
Yes, we provide necessary documentation including COA (Certificate of Analysis) and other regulatory dossiers to support product registration in various international markets.
4. What is the typical shelf life of these medications?
Most of our injection and tablet products have a shelf life of 24 to 36 months when stored under the recommended conditions (usually cool, dry places away from direct sunlight).
5. Are customized dosage strengths available?
We manufacture products based on standard international pharmacopoeia specifications. For specific volume requirements, please consult with our technical team regarding manufacturing capabilities.
6. How do you ensure the purity of Clindamycin and Metoclopramide injections?
Every batch undergoes rigorous HPLC testing and sterility checks in our quality control laboratories to ensure chemical purity and the absence of contaminants before release.

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