How to Source Acyclovir Cream (5%) for Pharmaceutical Formulation
Acyclovir Cream (5%) (Cream, Ointment, 5%) is classified under Derma Drugs. It is therapeutically aligned with reference brands such as Zovirax(US). This guide highlights key sourcing factors buyers should consider when procuring high-quality Acyclovir Cream (5%) for formulation, R&D, or bulk manufacturing.
Product Overview:
Acyclovir 5% cream is an antiviral that inhibits herpes simplex virus DNA replication by targeting viral DNA polymerase. It effectively reduces herpes outbreaks, alleviates symptoms, shortens healing time, and prevents virus spread. Benefits include faster lesion healing, less pain, and decreased recurrence when used as prescribed.
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
Acyclovir Cream (5%) 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 Acyclovir Cream (5%) 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 Acyclovir Cream (5%) is more than procurement—it’s a strategic partnership. With its cream, ointment form and 5% 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 Acyclovir Cream (5%).
Frequently Asked Questions For Sourcing of Acyclovir Cream (5%)
What is the typical lead time for Acyclovir Cream (5%)?
Lead times range from 4–6 weeks depending on supplier and region.
Is Acyclovir Cream (5%) available in multiple grades?
Yes — common grades include USP, EP, and JP. Verify grade suitability for your dosage form before purchase.
Does Acyclovir Cream (5%) require special storage?
It should be stored in a cool, dry place away from direct sunlight.
Is a Drug Master File (DMF) available for Acyclovir Cream (5%)?
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 Acyclovir Cream (5%)?
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 Acyclovir Cream (5%)?
Available documentation may include GMP, ISO 9001, ISO 14001, and ICH Q7 certificates, along with CoA, TDS, and stability data.
Is Acyclovir Cream (5%) suitable for regulated markets like US/EU?
Yes — compliant with EU/US/WHO GMP standards and available with regulatory support documentation for filings.
Can Acyclovir Cream (5%) be used in fixed-dose combinations?
Yes — many formulations support inclusion in FDCs. Compatibility studies and formulation consultation are available on request.
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