How to Source Valsartan & Hydrochlorothiazide Tablets for Pharmaceutical Formulation
Valsartan & Hydrochlorothiazide Tablets (Tablets, 80 + 12.5 mg, 160 + 12.5 mg) is classified under Hypertension. It is therapeutically aligned with reference brands such as Various Indian Brand Available. This guide highlights key sourcing factors buyers should consider when procuring high-quality Valsartan & Hydrochlorothiazide Tablets for formulation, R&D, or bulk manufacturing.
Product Overview:
Valsartan and Hydrochlorothiazide Tablet is used mainly to treat high blood pressure. Valsartan works by blocking the activity of certain natural substances which tightens the blood vessels. Thus, the blood flows more smoothly, and the heart pumps more efficiently and showing its results. Hydrochlorothiazide works by prompting the kidneys to pass the unneeded salt and water from the body into the urine.
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
Valsartan & Hydrochlorothiazide 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 Valsartan & Hydrochlorothiazide 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 Valsartan & Hydrochlorothiazide Tablets is more than procurement—it’s a strategic partnership. With its tablets form and 80 + 12.5 mg, 160 + 12.5 mg 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 Valsartan & Hydrochlorothiazide Tablets.
Frequently Asked Questions For Sourcing of Valsartan & Hydrochlorothiazide Tablets
What is the typical lead time for Valsartan & Hydrochlorothiazide Tablets?
Lead times range from 4–6 weeks depending on supplier and region.
Is Valsartan & Hydrochlorothiazide Tablets available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Valsartan & Hydrochlorothiazide 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 Valsartan & Hydrochlorothiazide 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 Valsartan & Hydrochlorothiazide 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 Valsartan & Hydrochlorothiazide Tablets?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Valsartan & Hydrochlorothiazide 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 Valsartan & Hydrochlorothiazide Tablets be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.