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Buy Diclofenac Sodium API in Colombia | WHO GMP Certified India Supplier
Buy Diclofenac Sodium API in Colombia — WHO GMP Certified India Supplier
Looking to buy Diclofenac Sodium API in Colombia? Aarise Pharmaceuticals is a WHO GMP certified Diclofenac Sodium API manufacturer based in Haridwar, India, supplying 99.0% purity USP/BP/IP grade Diclofenac Sodium (CAS 15307-79-6) to pharmaceutical buyers in Colombia with full INVIMA-compliant documentation.
Why Buy Diclofenac Sodium API from Aarise for Colombia?
- WHO GMP Certified — our Haridwar facility is WHO GMP certified, accepted by INVIMA
- Pharmacopeial Grade — USP/BP/IP grade, 99.0% purity, NABL-accredited QC testing
- Full INVIMA Documentation — COA, MSDS, COPP, DMF support, Certificate of Origin
- Competitive Pricing — direct manufacturer, no middlemen, best ex-works rates
- Fast Delivery — air freight 3-7 days to Colombia; 5-7 days lead time
- Small MOQ — from 1 kg; samples from 10g available
Diclofenac Sodium API Specifications
| Parameter | Specification |
|---|---|
| Chemical Name | Diclofenac Sodium |
| CAS Number | 15307-79-6 |
| Purity | 99.0% (USP/BP/IP) |
| Therapeutic Category | NSAID |
| Primary Use | Pain, inflammation and arthritis treatment |
| Dosage Forms | tablets, injections, gel, eye drops |
| MOQ | 1 kg |
| Lead Time | 5-7 days |
| Packaging | HDPE drums / double polylined fibre drums |
Buying Diclofenac Sodium API in Colombia — Regulatory Requirements
To import Diclofenac Sodium API into Colombia, buyers must comply with INVIMA (Instituto Nacional de Vigilancia de Medicamentos y Alimentos) requirements: INVIMA sanitary registration, WHO GMP certificate acceptance for bulk APIs, local importer or distributor required. Aarise Pharmaceuticals provides all required documentation to support your INVIMA import clearance.
Documentation Provided with Every Order
- Batch-specific Certificate of Analysis (COA) — signed by QC head
- MSDS / SDS in GHS format (English)
- WHO GMP Certificate (current)
- Certificate of Pharmaceutical Product (COPP)
- DMF support for INVIMA
- Certificate of Origin
- Stability data and shelf-life documentation
- Packing list and commercial invoice
How to Place an Order
- Contact Aarise Pharmaceuticals at +91 9899783330 or submit an inquiry online
- Receive a proforma invoice with pricing and delivery terms
- Request a free sample (10-50g) for your QC team evaluation
- Confirm the order and receive complete regulatory documentation
- Shipment dispatched within 5-7 days — air freight to Colombia in 3-7 days
Ready to buy Diclofenac Sodium API for Colombia? Contact us at +91 9899783330 or +91 9289410333 for pricing, samples, and a INVIMA-compliant documentation pack. We respond within 24 hours.
Frequently Asked Questions
Where can I buy Diclofenac Sodium API in Colombia?
You can buy Diclofenac Sodium API (CAS 15307-79-6) for Colombia directly from Aarise Pharmaceuticals, a WHO GMP certified manufacturer in Haridwar, India. We supply INVIMA-compliant Diclofenac Sodium API with full COA, MSDS, and DMF documentation. Contact us at +91 9899783330.
What is the price of Diclofenac Sodium API in Colombia?
The price of Diclofenac Sodium API for Colombia depends on quantity, grade (USP/BP/IP), and delivery terms. MOQ starts from 1 kg. Contact Aarise Pharmaceuticals for an ex-works price and CIF Colombia quote.
Is Diclofenac Sodium API available for import into Colombia?
Yes. Aarise Pharmaceuticals exports Diclofenac Sodium API to Colombia with full INVIMA-compliant documentation including WHO GMP certificate, COA, MSDS, COPP, and DMF support. We have experience with INVIMA import requirements.
What documentation is provided when buying Diclofenac Sodium API for Colombia?
Every order includes: batch-specific COA, WHO GMP certificate, MSDS/SDS (GHS format), COPP, Certificate of Origin, DMF support for INVIMA, and stability data. All documents are provided in English and formatted for INVIMA submission.
What is the minimum order quantity to buy Diclofenac Sodium API?
Minimum order quantity for Diclofenac Sodium API is 1 kg. Samples from 10-50g are available for QC evaluation and regulatory filing. Lead time is 5-7 days from order confirmation.