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Buy Diclofenac Sodium API in South Korea | WHO GMP Certified India Supplier

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Buy Diclofenac Sodium API in South Korea — WHO GMP Certified India Supplier

Looking to buy Diclofenac Sodium API in South Korea? 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 South Korea with full MFDS-compliant documentation.

Why Buy Diclofenac Sodium API from Aarise for South Korea?

  • WHO GMP Certified — our Haridwar facility is WHO GMP certified, accepted by MFDS
  • Pharmacopeial Grade — USP/BP/IP grade, 99.0% purity, NABL-accredited QC testing
  • Full MFDS 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 South Korea; 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 South Korea — Regulatory Requirements

To import Diclofenac Sodium API into South Korea, buyers must comply with MFDS (Ministry of Food and Drug Safety) requirements: MFDS API import notification, WHO GMP certificate, Korean-language labelling compliance, local importer registration. Aarise Pharmaceuticals provides all required documentation to support your MFDS 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 MFDS
  • Certificate of Origin
  • Stability data and shelf-life documentation
  • Packing list and commercial invoice

How to Place an Order

  1. Contact Aarise Pharmaceuticals at +91 9899783330 or submit an inquiry online
  2. Receive a proforma invoice with pricing and delivery terms
  3. Request a free sample (10-50g) for your QC team evaluation
  4. Confirm the order and receive complete regulatory documentation
  5. Shipment dispatched within 5-7 days — air freight to South Korea in 3-7 days

Ready to buy Diclofenac Sodium API for South Korea? Contact us at +91 9899783330 or +91 9289410333 for pricing, samples, and a MFDS-compliant documentation pack. We respond within 24 hours.

Frequently Asked Questions

Where can I buy Diclofenac Sodium API in South Korea?

You can buy Diclofenac Sodium API (CAS 15307-79-6) for South Korea directly from Aarise Pharmaceuticals, a WHO GMP certified manufacturer in Haridwar, India. We supply MFDS-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 South Korea?

The price of Diclofenac Sodium API for South Korea 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 South Korea quote.

Is Diclofenac Sodium API available for import into South Korea?

Yes. Aarise Pharmaceuticals exports Diclofenac Sodium API to South Korea with full MFDS-compliant documentation including WHO GMP certificate, COA, MSDS, COPP, and DMF support. We have experience with MFDS import requirements.

What documentation is provided when buying Diclofenac Sodium API for South Korea?

Every order includes: batch-specific COA, WHO GMP certificate, MSDS/SDS (GHS format), COPP, Certificate of Origin, DMF support for MFDS, and stability data. All documents are provided in English and formatted for MFDS 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.