SourcingAI

Paroxetine

I have found results from100+products and40+suppliers aboutParoxetine

Commonly Used:
US$
Customization Available
Sample Available
Manufacturer First
Product Attributes:
Type: Pharmaceutical Intermediates
Powder: Yes
Customized: Non-Customized
Certification: ISO 9001
Suitable for: Elderly
State: Solid
Purity: >99%
Feature: Stocked
Organic Chemical Material
Status: Solid State
Appearance: Powder
Quality: Refined
Colour: White
Function: Antineoplastic
Grade Standard: Medicine Grade
Volatile: Not Volatile
Age Group: Adults
Gender: Unisex
With Logo Printing
Product Type: Food
Classification: Substituted Benzenes
Shape: Powdery
Source: Petroleum
Customized: Customized
Certification: USP
Certification: BP
Certification: GMP
Certification: HSE
Certification: ISO
Certification: HACCP
Certification: QS
Certification: KOSHER
Certification: NOP
Certification: JAS
Certification: OCIA
Suitable for: Adult
Suitable for: Children
Purity: >96%
Feature: Organic
Feature: Vitamins
Feature: Low-Fat
Feature: Sugar-Free
Feature: Decaffeinated
Feature: Low-Salt
Feature: Glucose
Quality: Industrial
Grade Standard: Industrial Grade

Sourcing guidance for Paroxetine

What are the essential quality standards and certifications for sourcing Paroxetine API?

When sourcing Paroxetine as an Active Pharmaceutical Ingredient (API), you must ensure the supplier holds a GMP (Good Manufacturing Practice) certification. It is critical to verify if the product complies with international pharmacopoeia standards such as USP (United States Pharmacopeia), BP (British Pharmacopeia), or EP (European Pharmacopoeia). Additionally, request a Certificate of Analysis (CoA) for every batch to confirm purity levels, typically requiring ≥98% or ≥99%, and check for CEP (Certificate of Suitability) or DMF (Drug Master File) registration numbers to facilitate regulatory filing.

What technical specifications should be prioritized for Paroxetine Hydrochloride?

Buyers should specify the physical form required, such as Paroxetine Hydrochloride Anhydrous or Paroxetine Hydrochloride Hemihydrate, as these have different solubility and stability profiles. Pay close attention to Particle Size Distribution (PSD), which affects the dissolution rate in finished dosage forms. Furthermore, ensure the impurity profile (including residual solvents and heavy metals) falls within the strict limits defined by ICH (International Council for Harmonisation) guidelines.

How should the packaging and storage conditions be managed for bulk Paroxetine?

Paroxetine is sensitive to light and moisture. It must be packed in double-layer PE bags inside fiber drums that are sealed and light-resistant. The storage environment must be a cool, dry, and well-ventilated area, typically maintained at controlled room temperature (20°C to 25°C). Ensure the supplier provides Material Safety Data Sheets (MSDS) to guide handlers on chemical stability and emergency procedures.

Cross-Border Procurement Risks and Compliance for Pharmaceuticals

What are the legal and regulatory requirements for importing Paroxetine?

Pharmaceuticals are highly regulated. You must possess a valid Import License for prescription drugs in your destination country. Ensure the supplier is registered with the relevant health authorities (e.g., FDA, EMA, or NMPA). Failure to provide a Health Certificate or Export Declaration from the country of origin can lead to customs seizure or heavy fines.

How can I ensure transaction security and supplier reliability?

Use secure payment methods and consider third-party factory audits to verify the supplier's production capacity and quality control systems. On platforms like Made-in-China.com, prioritize Audited Suppliers who have undergone on-site verification. It is highly recommended to request a small sample for lab testing before committing to a full-scale commercial order to mitigate the risk of sub-standard materials.

What are the logistics and shipping precautions for Paroxetine?

Since Paroxetine is a chemical substance, it must be shipped with a Non-Dangerous Goods Certificate or a DGD (Dangerous Goods Declaration) if applicable. Choose freight forwarders experienced in cold chain or climate-controlled logistics to prevent degradation during transit. Always include insurance coverage for high-value pharmaceutical shipments to protect against loss or damage during cross-border transport.

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