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Buy Atorvastatin Calcium API in Brazil | WHO GMP Certified India Supplier
Buy Atorvastatin Calcium API in Brazil — WHO GMP Certified India Supplier
Looking to buy Atorvastatin Calcium API in Brazil? Aarise Pharmaceuticals is a WHO GMP certified Atorvastatin Calcium API manufacturer based in Haridwar, India, supplying 98.0% purity USP/BP grade Atorvastatin Calcium (CAS 134523-03-8) to pharmaceutical buyers in Brazil with full ANVISA-compliant documentation.
Why Buy Atorvastatin Calcium API from Aarise for Brazil?
- WHO GMP Certified — our Haridwar facility is WHO GMP certified, accepted by ANVISA
- Pharmacopeial Grade — USP/BP grade, 98.0% purity, NABL-accredited QC testing
- Full ANVISA 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 Brazil; 7-10 days lead time
- Small MOQ — from 1 kg; samples from 10g available
Atorvastatin Calcium API Specifications
| Parameter | Specification |
|---|---|
| Chemical Name | Atorvastatin Calcium |
| CAS Number | 134523-03-8 |
| Purity | 98.0% (USP/BP) |
| Therapeutic Category | Cardiovascular / Statin |
| Primary Use | Cholesterol reduction |
| Dosage Forms | tablets |
| MOQ | 1 kg |
| Lead Time | 7-10 days |
| Packaging | HDPE drums / double polylined fibre drums |
Buying Atorvastatin Calcium API in Brazil — Regulatory Requirements
To import Atorvastatin Calcium API into Brazil, buyers must comply with ANVISA (Agencia Nacional de Vigilancia Sanitaria) requirements: ANVISA GMP certification or WHO GMP acceptance, local importer registration, ANVISA product registration for finished goods. Aarise Pharmaceuticals provides all required documentation to support your ANVISA 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 ANVISA
- 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 7-10 days — air freight to Brazil in 3-7 days
Ready to buy Atorvastatin Calcium API for Brazil? Contact us at +91 9899783330 or +91 9289410333 for pricing, samples, and a ANVISA-compliant documentation pack. We respond within 24 hours.
Frequently Asked Questions
Where can I buy Atorvastatin Calcium API in Brazil?
You can buy Atorvastatin Calcium API (CAS 134523-03-8) for Brazil directly from Aarise Pharmaceuticals, a WHO GMP certified manufacturer in Haridwar, India. We supply ANVISA-compliant Atorvastatin Calcium API with full COA, MSDS, and DMF documentation. Contact us at +91 9899783330.
What is the price of Atorvastatin Calcium API in Brazil?
The price of Atorvastatin Calcium API for Brazil 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 Brazil quote.
Is Atorvastatin Calcium API available for import into Brazil?
Yes. Aarise Pharmaceuticals exports Atorvastatin Calcium API to Brazil with full ANVISA-compliant documentation including WHO GMP certificate, COA, MSDS, COPP, and DMF support. We have experience with ANVISA import requirements.
What documentation is provided when buying Atorvastatin Calcium API for Brazil?
Every order includes: batch-specific COA, WHO GMP certificate, MSDS/SDS (GHS format), COPP, Certificate of Origin, DMF support for ANVISA, and stability data. All documents are provided in English and formatted for ANVISA submission.
What is the minimum order quantity to buy Atorvastatin Calcium API?
Minimum order quantity for Atorvastatin Calcium API is 1 kg. Samples from 10-50g are available for QC evaluation and regulatory filing. Lead time is 7-10 days from order confirmation.