How to Source Acetyl Salicylic Acid + Magnesium Hydroxide Tablets for Pharmaceutical Formulation
Acetyl Salicylic Acid + Magnesium Hydroxide Tablets (Tablets, 75mg + 15.20mg) is classified under Analgesic. It is therapeutically aligned with reference brands such as Cardiomagnyl. This guide highlights key sourcing factors buyers should consider when procuring high-quality Acetyl Salicylic Acid + Magnesium Hydroxide Tablets for formulation, R&D, or bulk manufacturing.
Product Overview:
It has anti-inflammatory, analgesic and antipyretic activity. Magnesium hydroxide, which is part of Cardiolife, protect the gastrointestinal mucosa against acetylsalicylic acid. After oral administration, acetylsalicylic acid is absorbed from the gastrointestinal tract almost completely.
1. Regulatory Compliance & Documentation
Ensure suppliers provide:
- ✔ Valid DMF (Drug Master File)
- ✔ COA (Certificate of Analysis) for each batch
- ✔ GMP, ISO, or ICH Q7 compliance certificates
2. Purity, Grade & Specification Matching
Acetyl Salicylic Acid + Magnesium Hydroxide Tablets must meet exact grade and purity for your dosage form:
- ✔ USP / EP / JP grade verification
- ✔ Particle size distribution check
- ✔ Residual solvent and heavy metal limits
3. Supplier Reliability & Audit History
- ✔ Positive past audit reports
- ✔ Pharma client references
- ✔ Years of proven API manufacturing experience
4. Commercial Terms: Pricing, MOQ & Flexibility
- ✔ Transparent pricing
- ✔ Pilot batch MOQ flexibility
- ✔ Volume-based discounts
5. Lead Time, Inventory & Logistics
Typical lead time for Acetyl Salicylic Acid + Magnesium Hydroxide Tablets is 4–6 weeks.
- ✔ Emergency dispatch options
- ✔ Regional warehousing
- ✔ Special storage if needed
6. Formulation Support
- ✔ Technical datasheets
- ✔ Sample availability
- ✔ Stability study support
Conclusion
Sourcing Acetyl Salicylic Acid + Magnesium Hydroxide Tablets is more than procurement—it’s a strategic partnership. With its tablets form and 75mg + 15.20mg specification, choosing a compliant supplier ensures consistent quality and regulatory approval. Prioritize documentation, verify compatibility, and build relationships with transparent, reliable suppliers to secure long-term success.
Next Step: Get expert assistance in sourcing Acetyl Salicylic Acid + Magnesium Hydroxide Tablets.
Frequently Asked Questions For Sourcing of Acetyl Salicylic Acid + Magnesium Hydroxide Tablets
What is the typical lead time for Acetyl Salicylic Acid + Magnesium Hydroxide Tablets?
Lead times range from 4–6 weeks depending on supplier and region.
Is Acetyl Salicylic Acid + Magnesium Hydroxide Tablets available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Acetyl Salicylic Acid + Magnesium Hydroxide Tablets require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Acetyl Salicylic Acid + Magnesium Hydroxide Tablets?
Yes, a DMF is available for regulated markets upon request. It includes detailed quality, manufacturing, and stability data.
Can I request samples or a pilot batch of Acetyl Salicylic Acid + Magnesium Hydroxide Tablets?
Yes — pilot batches or samples can be arranged for R&D, stability studies, or formulation trials. MOQ may vary based on region and regulatory scope.
What compliance certificates are available for Acetyl Salicylic Acid + Magnesium Hydroxide Tablets?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Acetyl Salicylic Acid + Magnesium Hydroxide Tablets suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Acetyl Salicylic Acid + Magnesium Hydroxide Tablets be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.